Likes Subject
"I certainly hope the people who purchased the k9narc 10/22/22 9:05 AM
Here is what's coming from Deitsch and NPHC cngreen 07/08/22 10:28 AM
This board is for discussing NPHC. k9narc 03/31/18 11:17 AM
It is what I have said many times. Luna Tic 12/06/22 11:59 PM
There is only a few that still believe I-Glow 12/06/22 5:35 PM
Luna, I read that in Federal Court 97% I-Glow 12/06/22 2:24 PM
Has Deitsch gone into hiding? But it is I-Glow 12/06/22 12:29 PM
I would guess it was a MM buy I-Glow 11/29/22 3:05 PM
Yep.... Here's their sign.
k9narc 11/24/22 7:14 PM
But someone still bought. cngreen 11/24/22 6:31 PM
It was probably a sell, and they let
k9narc 11/24/22 11:41 AM
I thought You could not purchase NPHC shares holter49 11/24/22 11:22 AM
Why won't my 2 mil get bought lol Brokemillwright 11/23/22 3:22 PM
Oops. Make that TD Ameritrade…. And someone ThatBobGuy 11/23/22 2:36 PM
According to TS Ameritrade, someone just bought 1,000,000 ThatBobGuy 11/23/22 12:33 PM
He desperation of some if incredible lol. 100% Brokemillwright 11/22/22 3:37 PM
Good luck with that theory. The se. Is cngreen 11/22/22 2:37 PM
Again in plain easy to understand English there cngreen 11/22/22 2:35 PM
Deitsch is screwed - the SEC already has I-Glow 11/22/22 2:32 PM
Deitsch is so ignorant of the Securities Laws I-Glow 11/22/22 2:24 PM
It seams to me that some are blaming RSI38 11/22/22 11:14 AM
more BS. even the SEC doesnt show anywhere cngreen 11/20/22 10:36 PM
Prove it. what an opinion that was. cngreen 11/20/22 10:34 PM
You know when the sec is getting nervous cngreen 11/20/22 10:32 PM
You aren't familiar with the Federal Court system I-Glow 11/20/22 9:36 PM
Stock manipulation of the price is illegal. "Market manipulation I-Glow 11/20/22 9:23 PM
Deitsch has a great deal of exposure to I-Glow 11/20/22 9:09 PM
And where is the "new info" in this RSI38 11/20/22 3:11 PM
Notification That Quarterly Report Will Be Submitted Late weaver 2 11/19/22 7:41 PM
"Deitsch is finished."....... k9narc 11/19/22 10:03 AM
Sec has a weak case. It scares them cngreen 11/18/22 7:54 PM
You are right - from the SEC: "On August I-Glow 11/18/22 7:34 PM
Weak case now that is funny - 2 I-Glow 11/18/22 7:28 PM
Still holding lowincome 11/17/22 1:55 PM
I disagree. The SEC has enough time invested k9narc 11/17/22 12:29 PM
I agree. Obviously I could be wrong, RANGOLEGEND 11/17/22 12:03 PM
The only thing the sec will want to cngreen 11/17/22 12:02 PM
Certainly one of many outcomes. Let’s see… RANGOLEGEND 11/17/22 10:30 AM
If Deitsch is lucky the settlement will be I-Glow 11/17/22 10:26 AM
It's not true that it's at or below Knkn 11/16/22 6:56 PM
Meanwhile the CE is still on as I RSI38 11/16/22 6:40 PM
They can, but didn’t. I agree with you RANGOLEGEND 11/15/22 9:15 PM
You do understand that the SEC can also I-Glow 11/15/22 7:28 PM
Um, yeah, I think I debunked that RANGOLEGEND 11/15/22 7:19 PM
I would listen to Luna as she is I-Glow 11/15/22 7:15 PM
Thanks for the warning. I'm going to buy Knkn 11/15/22 3:39 PM
NPHC - Goofy R 11/15/22 3:16 PM
NPHC - The Long and Dirty History of Goofy R 11/15/22 3:16 PM
HoW'S THAT "RUN" GOING FOR YOU CNGREEN!?--.0001--HILARIOUS!!! Goofy R 11/15/22 2:19 PM
Here's the real threat: Luna Tic 11/12/22 11:43 PM
Issue of 12 Jurors. Wrong then; wrong now. Luna Tic 11/11/22 6:17 PM
Yes, 2018 is ancient history. Our RANGOLEGEND 11/11/22 9:24 AM
Likes Subject

03/31/18 11:17 AM
Luna Tic
12/06/22 11:59 PM
12/06/22 5:35 PM
12/06/22 2:24 PM
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11/29/22 3:05 PM
11/24/22 7:14 PM
11/24/22 6:31 PM
11/24/22 11:41 AM
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11/22/22 3:37 PM
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Nutra Pharma Corp. (NPHC)

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Moderators k9narc cngreen Luna Tic

Nutra Pharma Corp. (OTC: NPHC) is a biopharmaceutical company engaged in the acquisition, licensing and marketing of homeopathic treatments and ethical drugs for the management of pain, neurological disorders, cancer, auto-immune and infectious diseases. Nutra Pharma, through its RectoPharm subsidiary, carries out basic drug discovery research and clinical development and also seeks strategic licensing partnerships to reduce the risks associated with the drug development process ReceptoPharm is developing technologies for the production of drugs for HIV and multiple sclerosis (MS), and also offers small and start-up biotech companies a full range of contract research services.


Investment Highlights

  • Tapping into the OTC and the Therapeutic Markets
    Dual Approach Minimizes Risk to Investors
    Revenue Generating OTC Business
    12 FDA-Registered OTC Products in the U.S.
    Aggressively Advancing Therapeutic Pipeline
    IP Portfolio Includes 12 Patents & Patents Pending
    Designated US-FDA Orphan Drug Status for RPI-78M
    Management Team with Deep Relevant Experience


Corporate Strategy

Nutra Pharma's over-the-counter (OTC) products allow the company to achieve profitability and fund longer-term clinical trials in the therapeutic area. The therapeutics address a market size of > $10 billion, while the OTC products segment addresses a market size of $200 million - $500 million.

Reducing Risk

Nutra Pharma's strategy aims to optimize risk and return. At present, the company has a line of OTC products that bring in cash. This revenue will not only help fund development of the company's therapeutic line but, since sales of the OTC line and therapeutic line are uncorrelated, will result in a smoother revenue stream. By having what is, essentially, two businesses under one roof, Nutra Pharma mitigates risk to shareholders.

Revenue in the Short-term from OTC products

The OTC line comprises a number of analgesics. In October 2009, Nutra Pharma launched its first, called Cobroxin®, an over-the-counter pain reliever designed to treat moderate to severe chronic pain. In May 2010, the company launched its second consumer product, called Nyloxin®, an over-the-counter pain reliever that is a stronger version of Cobroxin.® And in December 2014, it launched Pet Pain-Away, an over-the-counter pain reliever designed to treat pain in cats and dogs. Nyloxin is currently being distributed both domestically and internationally via network marketing through the nationwide distributor Lumaxa.

Maximizing Return with a High-Value Therapeutic Line

Through its wholly owned subsidiary, ReceptoPharm, Inc., Nutra Pharma conducts drug discovery research and development activities. Nutra Pharma's R&D pipeline consists of several novel therapies in various stages of development to prevent and or treat multiple sclerosis (MS), human immunodeficiency virus (HIV), adrenomyeloneuropathy (AMN), herpes, and rheumatoid arthritis (RA). And the company is pursuing, aggressively, regulatory approval for these treatments.



Nyloxin is an anti-inflammatory, non-toxic, non-narcotic, non-addictive, non-steroidal analgesic designed for chronic pain relief. It was first launched as an oral spray for treating back pain, neck pain, headaches, joint pain, migraines, and neuralgia, and as a topical gel for treating joint pain, arthritis pain and pain from repetitive stress.

Since the beginning of 2014, it has been moved by the over 3,000 distributors in the Lumaxa network. Nutra Pharma is approved to distribute Nyloxin in India and is currently negotiating with large distributors throughout the region. Nutra Pharma is also working with several potential distributors in China and expects orders in India and China in the near future.

Nyloxin is clinically proven to treat Stage 2 (moderate to severe) and Stage 3 (severe) chronic pain. It is safe, non-narcotic and non-addictive, and does not impair cognitive function. Nyloxin is available in three strengths and 12 SKUs. In Regular Strength, Nyloxin is offered as an oral spray, a topical roll-on, and a topical gel. These same three preparations are offered in Extra Strength. The company also plans a 'Military Strength' Nyloxin for U.S. government buyers and military personnel.

Nyloxin Advantage

  • Non-Opiate
    Safe & Effective
    Clinically Proven

Jeff Gottfurcht is the first person in the world with rheumatoid arthritis to scale Mount Everest. Jeff reached the summit on May 14, 2011. He took Nyloxin with him as his pain reliever of choice.



Nyloxin Topical Gel

I'm a massage therapist I have incorporated Nyloxin into my pain therapies with unbelievable results. I believe in this product so much that I became a distributor just so my clients can live pain free.

- Steve Smith

Nyloxin Extra Strength Topical Gel

I have never written a testimonial before. I have to tell you I am completely amazed at how well this product has worked for me. I have been on hydrocodone for years. Four days after taking this I have not needed it. I truly am shocked at the difference this has made in my pain. I have already reordered!

- Elyse Feldberg

Nyloxin Oral Spray

I am amazed at how well the Nyloxin spray has worked for me. I have had headaches for years, which sometimes turn to migrains. I have done biofeedback, been in the medical care of neurologists, and gone through testings, nothing I have tried has ever gotten rid of my headaches for any length of time, until I tried the Nyloxin spray. I even went to the mountains last weekend at 6,000 feet, for 3 days without a headache the whole time, I don't remember that ever happening. I am sold on this product.

- Nancy Leamons

*Some of the testimonials listed here may be from MyNyloxin Independent Entrepreneurs who may receive compensation which is received based on the sale of Nyloxin products."


Pet Pain-Away

Pets Owned in the U.S.: 95.6 million cats, 83.3 million dogs

The market for pain relief in dogs and cats is more than $200 million.

Millions of pets suffer from acute or chronic pain. While acute pain is a normal sensation triggered in the nervous system to alert your pet of possible injury and the need to take it easy, chronic pain is different, chronic pain persists. Pain signals keep firing in the nervous system for weeks, months, even years.

Historically, pain relief products for pets have been shown to cause other significant healthcare concerns and side effects.

Today, cobra venom is successfully being used for treating various forms of pain, autoimmune and neurological disorders. The Nutra Pharma subsidiary, ReceptoPharm, and other researchers have definitively proven that extracts from cobra venom contain constituents that control pain and inflammation in animals.

Pet Pain Away provides all-natural anti-inflammatory analgesic pain relief that is non-toxic, non-narcotic, non-steroidal and contains no aspirin or acetaminophen. Safe to use on pets, it treats conditions that cause chronic pain in animals.

  • Relieves Pain from Hip Dysplasia!
    Relieves Arthritis & Joint Pain!
    Relieves General Chronic Pet Pains!
    Homeopathic, All-Natural Ingredients!
    Non-Addictive & Non-Opiate!
    Hypoallergenic Chicken flavor

Current Medical Research of the Available Remedies

Current pain relief products for pets such as NSAIDs (just for dogs) such as Carprofen (Novox or Rimadyl), Deracoxib (Deramaxx), Etodolac (Etogesic), Firocoxib (Previcox), Meloxicam (Metacam ) or Tepoxalin ( Zubrin) have been shown to cause kidney, liver, or digestive problems. Cats do not tolerate NSAIDs of any kind well. The only approved NSAID for cats in the United States is meloxicam and it is only approved for a single post-surgical injection to relieve pain. The dose must be exactly correct for the cat's weight. If it is given longer to cats, it often causes severe kidney damage.

Other medications such as Amantadine, Gabapentin and Tramadol may cause upset stomach, decreased heart rate, panting, and constipation. Veterinarians may prescribe stronger opiates only for a short periods. They usually don't prescribe steroids for pain, as they can have serious side effects. Veterinarians are usually hesitant to utilize pain therapies in companion animals because of the following: significant side effects, including nausea, vomiting, drowsiness, itching, constipation and respiratory depression; buildup of tolerance to analgesic requiring higher dosage over time to experience same effect; addictive properties that include severe withdrawal symptoms.


Therapeutic Pipeline

ReceptoPharm's research and development pipeline consists of several novel therapies in various stages of development to prevent and or treat multiple sclerosis (MS), human immunodeficiency virus (HIV), adrenomyeloneuropathy (AMN), herpes, rheumatoid arthritis (RA) and pain.

Phase 1 (P-I), Phase 2 (P-II), Phase 3 (P-III)


RPI-78M is derived from alpha-cobratoxin (α-CTX) by an oxidative procedure. Alpha-cobratoxin is the primary neuroactive peptide found in the venom of Asiatic cobras, and it represents the single active ingredient in the formulation under investigation. RPI-78M compares favorably with competing products. It lacks measurable toxicity, but is still capable of attaching to and affecting the target site on the cells. This means that patients cannot overdose.

Following years of investigations in humans and animals, it has displayed no serious adverse side effects. Patients experience symptomatic improvements, usually within six months of therapy. RPI-78M is extremely stable and resistant to heat, and so has a long shelf life. The drug's stability has been determined to be over four years at room temperature. It is easy to administer as a daily intramuscular injection (mcg dosing). RPI-78M has completed two trials for its use to treat adrenomyeloneuropathy (AMN). And at present, there are about 300 multiple sclerosis patients on open-label trials with RPI-78M.



Nutra Pharma has received Orphan Drug Status from the FDA for RPI-78M as a candidate for the treatment of juvenile MS. Nutra Pharma is actively seeking collaborative research partners for early stage trials of RPI-78M in the treatment of juvenile multiple sclerosis (MS). The company has already been in contact with potential researchers, hospitals and sites of care for the purpose of moving forward with phase I/II clinical studies.

Nutra Pharma believes that RPI-78M provides an entirely new approach to the treatment of auto-immune diseases, including MS. As an immuno-modulating agent and not an immunosuppressive, RPI-78M could be a disruptive new drug entity in the autoimmune disease space. In previous open-label studies, RPI-78M has shown consistent symptomatic improvements within a period of less than six months in all stages of MS. The recently received Orphan Drug designation from the FDA allows the company to fast-track efforts through the clinical process. Based on existing clinical experience with RPI-78M, Nutra Pharma is confident that it can receive accelerated approval in a relatively short time-frame (expected in as little as 22-26 months).




Market Opportunity

According to the Centers for Disease Control and Prevention (CDC), there are currently about 1.2 million persons in the United States over the age of 13 who are human immunodeficiency virus (HIV) infected. Over the past 10 years the number of people living with HIV has increased. The incidence of new HIV infections has remained fairly stable, however, at about 50,000 new cases every year. As yet there is no cure for HIV: no compound has been isolated that kills the pathogen. But antiretroviral therapies (ART) can reduce the ability of the virus to reproduce and so keep infection at a level that does not overwhelm the immune system. The World Health Organization (WHO) estimates that, currently, there are about 37 million people worldwide living with HIV. The market size of antiretroviral therapies is estimated to be around $15 billion.

Like HIV, multiple sclerosis (MS) occurs when the immune system malfunctions. MS develops when the immune system attacks the protective sheath (myelin) that covers nerve fibers and causes communication problems between the brain and the rest of the body. The National Multiple Sclerosis Society estimates that about 2.3 million people are affected by MS worldwide. The market size of the MS drug market is about $16.7 billion. Adrenoleukodystrophy (AMN), also known as Schilder's disease and sudanophilic leukodystrophy, is another condition in which the myelin sheath is damaged. The AMN market has the potential to reach $400 million after the launch of an effective treatment. The Herpes Simplex Virus (HSV) affects thousands. According to the CDC, in 2013, some 306,000 persons visited a doctor for the first time in connection with a herpes condition. And the CDC also reports that, in 2007, about 1.5 million people in the U.S. were living with rheumatoid arthritis.



Nutra Pharma is led by a management team comprised of highly experienced and educated professionals with a strong track record of excellence. This leadership is well-equipped to advance Nutra Pharma's therapeutic pipeline and increases distribution of its OTC products internationally.


Rik J. Deitsch - Chairman and Chief Executive Officer

Rik Deitsch holds both a B.S. in chemistry and an M.S. in biochemistry, and has conducted clinical and laboratory research in collaboration with scientists at Duke University Medical Center and the Cleveland Clinic. Deitsch is the author of two books and is an adjunct professor, teaching several courses for Florida Atlantic University's College of Business and Continuing Education Department.


Stewart Lonky, MD MBA - Director - Audit & Compensation Committees

Stewart Lonky is board certified in internal medicine, pulmonary and critical care medicine. He has published over a dozen articles in the peer-reviewed literature. Stewart is the former chief medical officer of a medical device company that developed diagnostic products for the early diagnosis of cervical and oral cancer. In that role, his duties included the direction of clinical research and the ultimate clearance of three new diagnostic devices by the U.S. Food and Drug Administration (FDA).


Harold H. Rump - Director

Harold Rump holds a B.S. from the United States Naval Academy. He is the former president, and director of Biogenix, Inc., a company involved with research and development of antiviral peptides from cobra venoms, including clinical trials under FDA-issued Investigational New Drug applications.


Garry R. Pottruck, CPA - Director - Chairman, Audit & Compensation Committees

Garry Pottruck is a CPA and financial expert on the NPHC's board of directors. Previously he served as chief accounting officer/controller at Scopas Technology Company, Inc., a NASDAQ-listed, development stage biotechnology research and development organization. He was, also, a principal and manager in the firm Argy, Wiltse & Robinson, PC ("Argy"), headquartered in McLean, Virginia.


Nutra Pharma Corporation
12502 W. Atlantic Blvd
Coral Springs, FL 33071
Phone: (954) 509-0911

QualityStocks Investor Relations
3370 N. Hayden Rd. Suite 123-591
Scottsdale, AZ 85251
Phone: (480) 374-1336


Please see disclaimer on the QualityStocks website:


Contact :
phone 954-509-0911
12502 West Atlantic Bvld.
Coral Springs, FL 33071

Shares outstanding 442,185,921 as of May 23,2017.
Shares outstanding 1,233,519,298 as of July 20,2017.

Nutra Pharma Corp. (OTCBB: NPHC) is a biopharmaceutical company specializing in the acquisition, licensing and commercialization of pharmaceutical products and technologies for the management of neurological disorders, cancer, autoimmune and infectious diseases.

Nutra Pharma Corp. through its subsidiaries carries out basic drug discovery research and clinical development and also seeks strategic licensing partnerships to reduce the risks associated with the drug development process. The Company's holding, ReceptoPharm, Inc., is developing technologies for the production of drugs for HIV and Multiple Sclerosis ("MS"). The Company's subsidiary, Designer Diagnostics, is engaged in the research and development of diagnostic test kits designed to be used for the rapid identification of infectious diseases such as Tuberculosis (TB) and Mycobacterium avium-intracellulare (MAI).

Nutra Pharma continues to identify and acquire intellectual property and companies in the biotechnology arena.

Mission Statement
Nutra Pharma is dedicated to the success of its patients, customers, investors and business partners through its development and acquisition of innovative pharmaceutical and life science solutions that will improve the lives of people throughout the world.

ReceptoPharm is an innovative biopharmaceutical drug discovery company developing proprietary therapeutic protein products primarily for the prevention and treatment of viral, autoimmune and neurological diseases in humans, including Adrenomyeloneuropathy (AMN), Multiple Sclerosis (MS), Rheumatoid Arthritis (RA), Pain, and Myasthenia Gravis (MG), and Human Immunodeficiency Virus (HIV).

 Drug Development

The emphasis of ReceptoPharm's approach to drug discovery and the development of new therapeutic agents is based upon specialized receptor-binding proteins found in nature. » Learn More

 CRO Services

ReceptoPharm offers a full range of contract services catering to start-up and small biotechnology companies. These services include pre-production studies, contract manufacturing services, US & EU regulatory support, and quality systems/GMP certification.

» Learn More

ReceptoPharm is a wholly owned subsidiary of Nutra Pharma Corporation.


Designer Diagnostics is a biotechnology sales and marketing company founded for the sale of diagnostics testkits for infectious diseases.

 Designer Diagnostics Test Kits provide a highly cost effective, highly efficient, low infrastructure solution for identifying and testing sensitivity of Nontuberculous Mycobacteria (NTM) that are capable of utilizing paraffin wax as a sole carbon source or those that are hydrophobic. Additionally Designer Diagnostics provides an efficient solution for the rapid identification and sensitivity testing of Tuberculosis (TB).

Designer Diagnostics is a wholly owned subsidiary of Nutra Pharma Corporation.

 Cobroxin/Nyloxin TV Commercials and Advertising

Here is a YouTube clip from 2013 showing the product:

Here is a link to the new commercials scheduled to begin airing at the end of June, 2014:


Nutra Pharma Corp NHPC is a biotech company that is developing treatments for Adrenomyeloneuropathy (AMN), HIV, and Multiple Sclerosis.
Nutra Pharma is announcing  that a new company that has the exclusive rights to market and distribute the over the counter product Nyloxin has signed contracts to begin airing TV commercials beginning June 23rd 2014. The first contract includes 30,000 spots between 30 and 90 seconds on the following networks:

The initial rollout is thoughout South Florida, expanding through the Northwest and down into California in the coming months.







SOURCE: Nutra Pharma Corporation

Nutra Pharma Announces Contracts for Nyloxin Television Commercials
June 10, 2014

Nutra Pharma is announcing that has contracted for the rollout of television commercials for their marketing Campaign of the Company's over-the-counter (OTC) pain reliever, Nyloxin®.

Coral Springs, FL. – June 10, 2014 - Nutra Pharma Corp. (OTCPink: NPHC), a biotechnology company that is developing treatments for Adrenomyeloneuropathy (AMN), HIV and Multiple Sclerosis (MS), is announcing that, a new company that has the exclusive rights to market and distribute Nutra Pharma's over-the-counter (OTC) pain reliever, Nyloxin®, has signed contracts to begin airing television commercials beginning June 23rd. The advertisements focus on the benefits of Nyloxin®. The first contract includes over 30,000 spots to run throughout the Southeast Region from Comcast and AT&T U-Verse Cable providers. The ads are scheduled to run on the following channels: GOLF, LMN, CNBC, FOXN, MSNBC, NBCS, ESPN, ESPN2, TNT, FOXS, TWC, CNN, HALL, HGTV, TLC, HLN and LIFE.

"MyNyloxin has been working diligently with our creative team to get these commercials completed," stated Dalton Johnson, CEO of "The initial rollout is throughout the South Florida market with eventual expansion into the Northeast and California markets in the coming months," he continued. "We believe that these advertisements will capture the imagination of potential customers that need access to a superior pain relief product and should help grow sales in the short term," he concluded.

Nyloxin® is an over-the-counter (OTC) pain reliever clinically proven to treat moderate to severe (Stage 2) chronic pain.  Nyloxin® is currently available in the United States as an oral spray for treating back pain, neck aches, headaches, joint pain, migraines, and neuralgia, and as a topical gel for treating joint pain, neck pain, arthritis pain, and pain from repetitive stress. In addition to its everyday strength formulation, Nyloxin® is also offered in an extra strength formula for more advanced, Stage 3, chronic pain.

“MyNyloxin Distributors have been consistently increasing the public awareness of Nyloxin,” said Rik J Deitsch, Chairman and CEO of Nutra Pharma Corporation. “They will be targeting these commercials in areas that are expected to provide the widest market for our pain relief products, with the eventual rollout to the national stage over the next several months,” he concluded.

The commercials can be viewed online at:

About Nutra Pharma Corp.

Nutra Pharma Corporation operates as a biotechnology company specializing in the acquisition, licensing, and commercialization of pharmaceutical products and technologies for the management of neurological disorders, cancer, autoimmune, and infectious diseases, including Multiple Sclerosis (MS), Human Immunodeficiency Virus (HIV), Adrenomyeloneuropathy (AMN) and Pain. Additionally, the Company markets several drug products for sale for the treatment of pain under the brands Cobroxin® and Nyloxin®. For additional information about Nutra Pharma, visit: or

SEC Disclaimer

This press release contains forward-looking statements. The words or phrases "would be," "will allow," "intends to," "will likely result," "are expected to," "will continue," "is anticipated," "estimate," "project," or similar expressions are intended to identify "forward-looking statements." Actual results could differ materially from those projected in Nutra Pharma's ("the Company") business plan. The contract to run Nyloxin commercials should not be construed as an indication in any way whatsoever of the future value of the Company’s common stock or its financial value. The Company's filings may be accessed at the SEC's Edgar system at  Statements made herein are as of the date of this press release and should not be relied upon as of any subsequent date. The Company cautions readers not to place reliance on such statements. Unless otherwise required by applicable law, we do not undertake, and we specifically disclaim any obligation, to update any forward-looking statements to reflect occurrences, developments, unanticipated events or circumstances after the date of such statement.

Nyloxin // Chronic Pain Relief




Here are the Nyloxin Brands that are currently available:








12/10/09 Webinar from Rik J Deitsch, Chairman and CEO of Nutra Pharma Corporation:






Nutra Pharma (NPHC.OB) PATENTS

U.S. Patent No. 5,989,857, which was granted in November 1999 with 10 claims.

U.S. Patent No. 6,670,148, which was granted in December 2003, with 9 claims. The patent further describes the method for preparing a bioactive peptide (protein) found in cobra venom, in a stable, inactivated form, by treating the peptide with ozone.

Buccal Delivery System, on which a patent is pending. This application describes a throat spray that permits efficient delivery of the modified peptide drugs to the body through oral mucosa.

Technology contained in one pending U.S. patent application for the further development of bioactive peptides in cobra venom for use in the treatment of HIV and MS.

Technology contained in two pending U.S. patent applications for Immunokine Composition and Method, which describes a method for developing modified peptides from alpha-cobratoxin.

Technology contained in two patents pending for the topical delivery of our proprietary wound healing treatment, which was developed in conjunction with Bio Therapeutics. One of these products is in the form of an ointment style skin protectant and the other a foaming aerosol.


R&D Pipeline

ReceptoPharm's research and development pipeline consists of several novel therapies in various stages of development to prevent and/or treat Multiple Sclerosis (MS), Human Immunodeficiency Virus (HIV), Adrenomyeloneuropathy (AMN), Herpes, Rheumatoid Arthritis (RA) and Pain.





In Progress





Preclinical (PC), Phase 1 (P-I), Phase 2 (P-II), Phase 3 (P-III)









Multiple Sclerosis






Herpes Simplex Infections 1 & 2












Adrenomyeloneuropathy (Oral)













Human Immunodeficiency Virus (Oral)






Human Immunodeficiency Virus






Amyotrophic Lateral Sclerosis






Herpes Simplex Keratitis













Rheumatoid Arthritis














Regulatory Status


Chronic Pain (OTC)




Cobroxin for Chronic Pain


Cobroxin is the first over-the-counter pain reliever clinically proven to treat moderate to severe (Stage 2) chronic pain. The drug will be available as an oral spray for treating lower back pain, migraines, neck aches, shoulder pain, cramps and neuralgia and as a topical gel for treating joint pain and pain associated with repetitive stress and arthritis. For more information, visit




Regulatory Status


Chronic Pain (OTC)

Undergoing International Registrations


Chronic Pain (Rx)

Undergoing International Registrations



Nyloxin // Chronic Pain Relief


Nyloxin is a treatment for moderate to severe chronic pain. The over-the-counter formulation, Nyloxin OTC, is aimed at treating moderate to severe (Stage 2) chronic pain. The prescription strength formulation, Nyloxin Rx, is aimed at treating severe (Stage 3) chronic pain and is intended for distribution worldwide, including in the United States. For more information, visit


Nutra Pharma (NPHC.OB) Investor Information

Nutra Pharma Corp.
12502 West Atlantic Bvld.
Coral Springs, FL 33071

Nina Goldstein - Investor Relations
Toll-Free: (877) 895-5647

Transfer Agent

Standard Registrar and Transfer Co., Inc.
12528 South 1840 E.
Draper, UT 84020

Phone: (801) 571-8844

Nutra Pharma Corp. (OTC: NPHC.OB)

is a fully reporting OTC stock



During our second quarter of 2015 and thereafter, the following has occurred:

On April 15, 2015 we provided an update regarding plans to market Nyloxin® through S.Zhaveri Pharmakem for distribution throughout India. The update stated that our management had been working in Mumbai throughout the week to finalize plans for the national rollout of Nyloxin®.

On April 20, 2015, our stockholders voted at a special meeting of the shareholders held in Coral Springs, Florida to approve a one-for-forty reverse stock split of our issued and outstanding shares of common stock.   Under the adopted proposal, each forty shares of our presently issued and outstanding Common Stock as of the close of business on the effective date was converted automatically into one share of our post-Reverse Split Common Stock. Fractional shares and "odd lots" were rounded up to the nearest whole share. The Reverse Split did not change the number of authorized shares of our Common Stock. The principal effect of the Reverse Split was the reduction in the number of shares of Common Stock issued and outstanding, from 1,510,950,321 shares as of March 6, 2015 to 39,123,758 shares after the Reverse Split was deemed effective. The Reverse Split affected all of our shareholders uniformly and did not affect any shareholder’s percentage ownership interest in Nutra or any shareholder’s proportionate voting power. Per share and weighted average amounts have been retroactively restated in the accompanying financial statements and related notes to reflect this stock split.

On April 22, 2015 we announced that we had engaged the Vancouver Commodities Group (VCG) to begin the process of identifying and vetting potential distributors in China for Nyloxin®.

On April 30, 2015 we announced that we had received notification of the acceptance of Nyloxin® by the China International Exchange and Promotive Association for Medical and Healthcare (CPAM). This process was successfully conducted by the Vancouver Commodities Group (VCG) that had been hired by Nutra Pharma to begin the process of identifying and vetting potential distributors in China.

On May 14, 2015 we announced that we had engaged the Nature's Clinic to begin the process of regulatory approval of our Company's Over-the-Counter pain drug, Nyloxin® for marketing and distribution in Canada. The Nature’s Clinic has already begun setting up their Chatham, Ontario warehouse and expect to complete the approval process to begin distributing Nyloxin® by the end of the year.

On May 26, 2015 we announced that we had engaged Medical Strategy Consultants, LLC to aid the company in the filing of Orphan Drug applications with the U.S. Food and Drug Administration ("FDA"). The first application under development is for the treatment of Pediatric Multiple Sclerosis with the Company's lead drug candidate, RPI-78M. In order to create the application, RPI-78M needed to meet several key criteria. This included preclinical data in support of the drug that provided a reasonable rationale for the treatment of the disease based on its potential ability to treat the symptoms of multiple sclerosis. The FDA grants Orphan Drug Designation status to products that treat rare diseases, providing incentives to sponsors developing drugs or biologics. The Orphan Drug Act of 1983 is intended to assist and encourage companies to develop safe and effective therapies for the treatment of rare diseases and disorders, defined as those affecting fewer than 200,000 Americans at any given time. The designation of RPI-78M as an Orphan Drug would provide Nutra Pharma with a 7-year period of market exclusivity in the U.S. upon approval of the drug, as well as tax credits for clinical research costs, the ability to apply for grant funding, clinical trial design assistance, assistance from the FDA in the drug development process and the waiver of Prescription Drug User Fee Act (PDUFA) filing fees which could be in excess of $2.5 million. The decision to proceed with an Orphan Drug Designation submission is part of Nutra Pharma's plan to move forward with the preparation of an Investigative New Drug Application.

On June 9, 2015 we announced that we had entered into a facility and personnel sharing agreement with Nationwide Laboratory Services, Inc. (NLS): Nationwide Laboratory Services, Inc. operates as a clinical diagnostics laboratory, performing routine and specialty human diagnostics. The company also offers clinical trial services, such as specimen and special handling requirements, status of test results, turnaround time, testing, participants test results, channeling calls to technical or professional personnel, communicating specimen issues, notifying investigational site of critical calls, and telephone support with data management training services; and courier tracking services. The collaboration provides NLS with the use of our lab space and equipment and provides us with lab and clinical personnel as well as cost-savings on rent and utilities.

On June 23, 2015 we announced that we had completed a series of projects to update and expand the facilities that house the Asian cobras utilized for the production of Nyloxin®. We also announced the addition of 100 snakes to the existing milking line to increase venom production for the upcoming international orders from India and China.

On June 30, 2015 we announced that we had engaged Pickwick Capital Partners; a leading investment banking, securities and investment management firm, to provide strategic corporate planning and investment banking services. Pickwick will focus on assisting Nutra Pharma in our strategies for maximizing shareholder value through its full scope of investment banking services.

On July 10, 2015, SeeThruEquity, a leading independent equity research and corporate access firm focused on smallcap and microcap public companies, announced it has initiated coverage of Nutra Pharma Corporation with a Price Target of $0.53 per share.

On July 15, 2015 we announced that we had filed an application with the FDA for orphan drug status of the Company's RPI-78M drug candidate for the treatment of Multiple Sclerosis in children. This represents the first such filing for the company.

 Moderator's Disclaimer - This board is for (NPHC) discussion purposes only and is in no way a recommendation to buy or sell. Any investment decisions should be based on your own due diligence and decision. You are solely responsible for your choices to buy or sell.


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