NYLOXIN description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

NYLOXIN

RECEPTOPHARM INC


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredients

Asian Cobra venom 60 mcg/mL

Purpose

AnalgesicAccording to the Homeopathic Pharmacopeia of the United States

Uses

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 Pharmacopeia of the United States.
  • 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 – 2.0 oz Gel Label

NYLOXIN

Package Label - Principal Display Panel – 2.0 oz Gel Carton

NYLOXIN

NYLOXIN

NAJA NAJA VENOM GEL

Product Information

Product Type Human otc drug label Item Code (Source) NDC:47219-253
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
NAJA NAJA VENOM Naja Naja Venom 60 ug

Inactive Ingredients

Ingredient Name Strength
DIPROPYLENE GLYCOL
benzalkonium chloride
2-(DIETHYLAMINO)ETHANOL
SODIUM CHLORIDE
hydroxypropyl cellulose

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 60 in 1 BOTTLE, DISPENSING
2 NDC:47219-253-20 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2009-08-25


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.