COBROXIN FOR CHRONIC PAIN- naja naja venom gel

COBROXIN by

Drug Labeling and Warnings

COBROXIN by is a Homeopathic medication manufactured, distributed, or labeled by RECEPTOPHARM INC, LIQUID PACKAGING RESOURCES. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

* According to the Homeopathic Pharmacopeia of the United States

Asian Cobra venom 5X *

Purpose

Analgesic

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.
• Press down on one side of top to open. Squeeze a small amount of gel into palm and rub vigorously into joints.
• Use 3-4 times per day for the 1st 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.

SPL UNCLASSIFIED SECTION

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

Inactive Ingredients:

Benzalkonium chloride, Methocel, Ethanol, Propylene glycol, Saline

PRINCIPAL DISPLAY PANEL

Package Label - Principal Display Panel – 1.0 oz Gel Label

PRINCIPAL DISPLAY PANEL

Package Label - Principal Display Panel – 1.0 oz Gel Carton

INGREDIENTS AND APPEARANCE

COBROXIN  FOR CHRONIC PAIN
naja naja venom gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47219-104
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NAJA NAJA VENOM (UNII: ZZ4AG7L7VM) (NAJA NAJA VENOM - UNII:ZZ4AG7L7VM)	NAJA NAJA VENOM	.020 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
DIPROPYLENE GLYCOL (UNII: E107L85C40)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
2-(DIETHYLAMINO)ETHANOL (UNII: S6DL4M053U)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47219-104-50	1 in 1 BOX
1		58 mL in 1 BOTTLE, DISPENSING

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Unapproved homeopathic		08/25/2009

Labeler - RECEPTOPHARM INC (145377888)

Establishment
Name	Address	ID/FEI	Business Operations
RECEPTOPHARM INC		145377888	ANALYSIS, MANUFACTURE, API MANUFACTURE

Establishment
Name	Address	ID/FEI	Business Operations
LIQUID PACKAGING RESOURCES		018935165	MANUFACTURE