BENGAY VANISHING SCENT- menthol, unspecified form gel 
Johnson & Johnson Consumer Inc.

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BENGAY ® VANISHING SCENT

Drug Facts

Active ingredient

Menthol 2.5%

Purpose

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. 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

camphor, carbomer, DMDM hydantoin, isoceteth-20, isopropyl alcohol, PEG-40 hydrogenated castor oil, sodium hydroxide, 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 - 57 g Tube Carton

VANISHING SCENT
MENTHOL 2.5% TOPICAL ANALGESIC GEL
BENGAY ®
With a scent that
starts to fade
in minutes

NET WT 2 OZ (57 g)

PRINCIPAL DISPLAY PANEL - 57 g Tube Carton
BENGAY VANISHING SCENT 
menthol, unspecified form gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0595
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM25 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
ISOCETETH-20 (UNII: O020065R7Z)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0595-21 in 1 CARTON04/03/2019
157 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01704/03/2019
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 10/2023
Document Id: 07d3cbc3-3465-d46d-e063-6294a90a0d58
Set id: 6cc3294b-3b0f-44d0-af71-61db1022d269
Version: 6
Effective Time: 20231016
 
Johnson & Johnson Consumer Inc.