BENGAY ARTHRITIS PAIN RELIEVING - menthol and methyl salicylate cream
Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredients	Purpose
Menthol 8%	Topical analgesic
Methyl salicylate 30%	Topical analgesic

Uses

temporarily relieves the minor aches and pains of muscles and joints associated with:

simple backache
arthritis
strains
bruises
sprains

Warnings

For external use only.

Do not use

on wounds or damaged skin
with a heating pad
on a child under 12 years of age with arthritis-like conditions

Ask a doctor before use if you have redness over the affected area.

When using this product

avoid contact with eyes or mucous membranes
do not bandage tightly

Stop use and ask a doctor if

condition worsens or symptoms persist for more than 7 days
symptoms clear up and occur again within a few days
excessive skin irritation occurs

Keep out of reach of children to avoid accidental ingestion. If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

use only as directed
adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily
children under 12 years of age: ask a doctor

Other information

store at 20° to 25°C (68° to 77°F)

Inactive ingredients

glyceryl stearate se, lanolin, methylparaben, potassium cetyl phosphate, potassium hydroxide, propylparaben, stearic acid, water

Questions?

call 1-800-223-0182

Dist: Johnson & Johnson Consumer Products Company
Division of Johnson & Johnson Consumer Companies Inc.
Skillman, NJ 08558 USA

PRINCIPAL DISPLAY PANEL - 57 g Tube Carton Label

ARTHRITIS FORMULA
NON-GREASY CREAM

BENGAY®
PAIN RELIEVING CREAM

NET WT 2 OZ (57 g)

PRINCIPAL DISPLAY PANEL - 57 g Tube Carton Label

BENGAY ARTHRITIS PAIN RELIEVING
menthol and methyl salicylate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:58232-4020
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Menthol (Menthol)	Menthol	80 mg in 1 g
Methyl Salicylate (Methyl Salicylate)	Methyl Salicylate	300 mg in 1 g

Inactive Ingredients
Ingredient Name	Strength
Glyceryl Stearate SE
Lanolin
Methylparaben
Potassium Cetyl Phosphate
Potassium Hydroxide
Propylparaben
Stearic Acid
Water

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Multilevel Packaging
1	NDC:58232-4020-1	1 TUBE ( TUBE) in 1 CARTON	contains a TUBE
1		57 g in 1 TUBE	This package is contained within the CARTON (58232-4020-1)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part348	05/23/2012

Labeler - Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. (830803164)

Revised: 05/2012 Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.