Label: BENGAY ULTRA STRENGTH NON-GREASY (camphor- synthetic, menthol, unspecified form, and methyl salicylate cream
- NDC Code(s): 69968-0538-2, 69968-0538-4, 69968-0538-5
- Packager: Johnson & Johnson Consumer Inc.
- Category: HUMAN OTC DRUG LABEL
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Updated July 15, 2022
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- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
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
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
- Other information
- Inactive ingredients
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 113 g Tube Carton
INGREDIENTS AND APPEARANCE
BENGAY ULTRA STRENGTH NON-GREASY
camphor (synthetic), menthol, unspecified form, and methyl salicylate cream
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0538 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength 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 FORM 100 mg in 1 g METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 300 mg in 1 g Inactive Ingredients Ingredient Name Strength 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0538-2 1 in 1 CARTON 06/01/2018 1 57 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:69968-0538-4 1 in 1 CARTON 06/01/2018 2 113 g in 1 TUBE; Type 0: Not a Combination Product 3 NDC:69968-0538-5 2 in 1 CARTON 06/01/2018 3 113 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 06/01/2018 Labeler - Johnson & Johnson Consumer Inc. (002347102)