Nyloxin
FDA Label NDC 47219-204

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Receptopharm Inc for the product Nyloxin (NDC 47219-204). 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, indications & usage, warnings:, directions for use:, other information:, other, inactive ingredients:, 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 5X

Purpose

Analgesic

According to the Homeopathic Pharmacopeia of the United States

Indications & Usage

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.

Directions For Use:

  • Remove protective wrapping.
  • Liberally apply gel to the affected area and rub into joints.
  • Use 3-4 times 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 mild to moderate (Stage 2) chronic pain, as indicated by the Homeopathic Pharmacopea of the United States.

Other

  • Pregnant or nursing women and children should not use this product unless advised by a physician

Inactive Ingredients:

Benzalkonium chloride, Ethanol, Methocel, Propylene glycol, Saline

Package Label.Principal Display Panel

Package Label - Principal Display Panel – 2.0 oz Gel Label

2.0 Oz Gel Bottle Label (Nyloxin Figure 1)

2.0 Oz Gel Bottle Label (Nyloxin Figure 1)

Package Label - Principal Display Panel – 2.0 oz Gel Carton

2.0 Oz Gel Bottle Carton (Nyloxin Figure 2)

2.0 Oz Gel Bottle Carton (Nyloxin Figure 2)

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