Nyloxin Gel
FDA Label NDC 47219-310

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Nutra Pharma Corporation for the product Nyloxin (NDC 47219-310). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredients, purpose, uses:, warnings:, otc - keep out of reach of children, directions for use:, other information:, otc - ask doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients

Asian Cobra Venom 4x (60 mcg/mL)

Purpose

Analgesic*
___________________________________________________________

*According to the Homeopathic Pharmacopeia of the United States

Uses:

Temporarily relieves joint pain associated with overuse and pain associated with arthritis.

Warnings:

- For external use only.

- If symptoms persist or worsen, discontinue use and seek medical attention.

- Avoid contact with eyes. If product gets into eyes flush with water. Seek Medical attention.

- Not for use on open wounds.


Otc - Keep Out Of Reach Of Children

Keep out of the reach of children

Directions For Use:

  • Remove protective wrapping
  • Liberally apply gel to the affected area and rub into joints.
  • Use 3-4 time per day for the first week. Use as needed thereafter to relieve discomfort.
  • Allow several days for drug to take maximum effect.

Other Information:

  • Do not use if container seal is broken prior to opening.
  • This product is intended for use in cases of recurring joint pain.
  • This product is NOT intended to treat disease, it provides a temporary level of comfort, relief and a feeling of wellness.
  • This product has been determined to be safe and effective for moderate to severe (Stage 2) chronic pain, as indicated by the Homeopathic Pharmacopeia of the United States.

Otc - Ask Doctor

  • Pregnant or nursing women and children should consult a physician before use.

Inactive Ingredients:

Benzalkonium chloride, Ethanol, Methocel, Propylene glycol, Saline.

Otc - Questions

For more information visit: www.Nyloxin.com

Manufactured by NutraPharma

2775 University Drive, Coral Springs, FL 33065 (954) 834-3740

Principal Display Panel

NDC 47219-310-02

Nyloxin Topical Gel Extra Strength

Easy Squeeze Bottle

Maximum Chronic Pain Relief

Topical Gel

30 DAY SUPPLY

* Please review the disclaimer below.