Nyloxin
FDA Label NDC 47219-203

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 47219-203). 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, directions:, warnings:, other, package label.principal display panel, 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

Purpose

Analgesic

Directions:

  • Break protective tab off.
  • Turn Press lock so spray nozzle is visible in front.
  • Press down on pump.
  • Spray directly into mouth or under tongue.

    • Use 2 sprays 4 times a day

    Note: It may take several days to induce relief. Use within 90 days of opening.
    Store at 50° to 80°F

Warnings:

For oral use only. Over use may induce headaches. Not for use by pregnant women. If symptoms persist, consult a physician.

Other

For more information visit
www.Nyloxin.com

Manufactured for: Nutra Pharma
Plantation, FL 33313

Package Label.Principal Display Panel

Package Label - Principal Display Panel – 0.5 oz Spray Label

0.5 Oz Spray Bottle Label (Nyloxin Figure 1)

0.5 Oz Spray Bottle Label (Nyloxin Figure 1)

* Please review the disclaimer below.