BENGAY ULTRA STRENGTH NON GREASY PAIN RELIEVING (camphor- synthetic, menthol, and methyl salicylate cream

Bengay Ultra Strength Non Greasy Pain Relieving by

Drug Labeling and Warnings

Bengay Ultra Strength Non Greasy Pain Relieving by is a Otc medication manufactured, distributed, or labeled by Johnson & Johnson Consumer Inc. . Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active ingredients	Purpose
Camphor 4%	Topical analgesic
Menthol 10%	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

carbomer, Disodium EDTA, glyceryl stearate se, lanolin, polysorbate 80, potassium hydroxide, purified water, stearic acid, Triethanolamine

Questions?

Call 1-800-223-0182 or 215-273-8755 (collect)

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 113 g Tube Carton

ULTRA STRENGTH
NON-GREASY CREAM

BENGAY®
PAIN RELIEVING CREAM

NET WT 4 OZ (113g)

INGREDIENTS AND APPEARANCE

BENGAY ULTRA STRENGTH NON GREASY PAIN RELIEVING 
camphor (synthetic), menthol, and methyl salicylate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58232-4024
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
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
Edetate Disodium (UNII: 7FLD91C86K)
Glyceryl Stearate se (UNII: FCZ5MH785I)
Lanolin (UNII: 7EV65EAW6H)
Polysorbate 80 (UNII: 6OZP39ZG8H)
Potassium Hydroxide (UNII: WZH3C48M4T)
Water (UNII: 059QF0KO0R)
Stearic Acid (UNII: 4ELV7Z65AP)
Trolamine (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58232-4024-3	1 in 1 CARTON	06/01/2008
1		57 g in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 58232-4024-5	1 in 1 CARTON	08/07/2012	09/01/2015
2		76 g in 1 TUBE; Type 0: Not a Combination Product
3	NDC: 58232-4024-1	1 in 1 CARTON	06/01/2008
3		113 g in 1 TUBE; Type 0: Not a Combination Product
4	NDC: 58232-4024-2	2 in 1 CARTON	06/01/2008
4		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	06/01/2008

Labeler - Johnson & Johnson Consumer Inc. (002347102)