BENGAY ULTRA STRENGTH NON-GREASY- camphor (synthetic), menthol, unspecified form, and methyl salicylate cream 
Johnson & Johnson Consumer 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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BENGAY ® ULTRA STRENGTH NON-GREASY CREAM

Drug Facts

Active ingredientPurpose
Camphor 4%Topical analgesic
Menthol 10%Topical analgesic
Methyl salicylate 30%Topical analgesic

Use

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 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. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

store at 20° to 25°C (68° to 77°F)

Inactive ingredients

carbomer, disodium EDTA, glyceryl stearate SE, lanolin, polysorbate 80, potassium hydroxide, stearic acid, triethanolamine, water

Questions?

call 1-800-223-0182 (toll-free) or 215-273-8755 (collect)

Distributed by:
JOHNSON & JOHNSON CONSUMER INC.
Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 113 g Tube Carton

ULTRA STRENGTH
TOPICAL ANALGESIC CREAM

BENGAY ®

With three
ingredients for
powerful relief
at the site of pain

Camphor 4%
Menthol 10%
Methyl
Salicylate 30%

NET WT 4 OZ (113 g)

PRINCIPAL DISPLAY PANEL - 113 g Tube Carton
BENGAY ULTRA STRENGTH NON-GREASY 
camphor (synthetic), menthol, unspecified form, and methyl salicylate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0538
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)40 mg  in 1 g
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM100 mg  in 1 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE300 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
LANOLIN (UNII: 7EV65EAW6H)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TROLAMINE (UNII: 9O3K93S3TK)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0538-21 in 1 CARTON06/01/2018
157 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:69968-0538-41 in 1 CARTON06/01/2018
2113 g in 1 TUBE; Type 0: Not a Combination Product
3NDC:69968-0538-52 in 1 CARTON06/01/2018
3113 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34806/01/2018
Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 7/2022
Document Id: e3d3abad-c2e7-da4c-e053-2995a90a7773
Set id: 0a41ec65-bd0b-4fc6-807d-74f353341cc7
Version: 5
Effective Time: 20220715
 
Johnson & Johnson Consumer Inc.