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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Arthritis Formula
BENGAY®
Pain Relieving Cream

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:

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

Other information

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 (UNII: L7T10EIP3A) (Menthol - UNII:L7T10EIP3A) Menthol 80 mg  in 1 g
Methyl Salicylate (UNII: LAV5U5022Y) (Salicylic Acid - UNII:O414PZ4LPZ) Methyl Salicylate 300 mg  in 1 g
Inactive Ingredients
Ingredient Name Strength
Glyceryl Stearate SE (UNII: FCZ5MH785I)  
Lanolin (UNII: 7EV65EAW6H)  
Methylparaben (UNII: A2I8C7HI9T)  
Potassium Cetyl Phosphate (UNII: 03KCY6P7UT)  
Potassium Hydroxide (UNII: WZH3C48M4T)  
Propylparaben (UNII: Z8IX2SC1OH)  
Stearic Acid (UNII: 4ELV7Z65AP)  
Water (UNII: 059QF0KO0R)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:58232-4020-1 1 in 1 CARTON
1 57 g in 1 TUBE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH NOT FINAL part348 05/23/2012 08/01/2017
Labeler - Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. (830803164)

Revised: 12/2012
Document Id: e0f67873-e7de-4756-9a95-9ddecac02eeb
Set id: d9d8ee70-8833-4424-b5a0-fcc375b514ec
Version: 2
Effective Time: 20121207
 
Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.