BENGAY VANISHING SCENT PAIN RELIEVING- menthol gel 
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.

----------

BENGAY® Vanishing Scent Menthol Pain Relieving Gel

Drug Facts

Active ingredient

Menthol 2.5%

Purpose

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

Directions

  • 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

Water, isopropyl alcohol, PEG-40 hydrogenated castor oil, carbomer, isoceteth-20, sodium hydroxide, DMDM hydantoin, camphor

Questions?

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

PRINCIPAL DISPLAY PANEL - 57 g Tube Carton

VANISHING SCENT

NON-GREASY GEL

BENGAY®
MENTHOL PAIN RELIEVING GEL

NET WT 2 OZ (57 g)

PRINCIPAL DISPLAY PANEL - 57 g Tube Carton
BENGAY VANISHING SCENT PAIN RELIEVING 
menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58232-4016
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RACEMENTHOL (UNII: YS08XHA860) (RACEMENTHOL - UNII:YS08XHA860) RACEMENTHOL25 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Isopropyl Alcohol (UNII: ND2M416302)  
Polyoxyl 40 Hydrogenated Castor Oil (UNII: 7YC686GQ8F)  
Isoceteth-20 (UNII: O020065R7Z)  
Sodium Hydroxide (UNII: 55X04QC32I)  
DMDM Hydantoin (UNII: BYR0546TOW)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58232-4016-31 in 1 CARTON11/30/200910/01/2018
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 NOT FINALpart34811/30/200910/01/2018
Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 9/2016
Document Id: 421a32a2-4c76-4192-86e6-2263bd644a57
Set id: bc34dc2a-fb50-4a58-8cdb-7d56426c6b37
Version: 3
Effective Time: 20160929
 
Johnson & Johnson Consumer Inc.