BENGAY COLD THERAPY  WITH PRO-COOL TECHNOLOGY- 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.

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BENGAY® Cold Therapy
Menthol Pain Relieving Gel

Drug Facts

Active ingredient

Menthol 5%

Purpose

Topical analgesic

Uses

temporarily relieves the minor aches and pains of muscles and joints associated with:

  • simple backache
  • bruises
  • arthritis
  • sprains
  • strains

Warnings

For external use only.

Flammable: Keep away from fire or flame.

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

alcohol, aminomethyl propanol, camphor, carbomer, disteareth-75 IPDI, ethylhexyl isononanoate, FD&C blue no. 1, glycerin, isopropyl alcohol, PEG-7 caprylic/capric glycerides, polysorbate 60, water

Questions?

call 1-800-223-0182

PRINCIPAL DISPLAY PANEL - 113g Tube Label

NEW

BENGAY®
menthol pain relieving gel

cold therapy
with PRO-COOL™ technology

cooling

FAST ACTING PAIN RELIEF

Same technology used
by chiropractors and
physical therapists

vanishing scent

NET WT 4 OZ (113g)

Principal Display Panel - 113g Tube Label
BENGAY COLD THERAPY   WITH PRO-COOL TECHNOLOGY
menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58232-4029
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Menthol, Unspecified Form (UNII: L7T10EIP3A) (Menthol, Unspecified Form - UNII:L7T10EIP3A) Menthol, Unspecified Form50 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
Alcohol (UNII: 3K9958V90M)  
Aminomethylpropanol (UNII: LU49E6626Q)  
Camphor (Synthetic) (UNII: 5TJD82A1ET)  
Ethylhexyl Isononanoate (UNII: I6KB4GE3K4)  
FD&C Blue No. 1 (UNII: H3R47K3TBD)  
Glycerin (UNII: PDC6A3C0OX)  
Isopropyl Alcohol (UNII: ND2M416302)  
Polysorbate 60 (UNII: CAL22UVI4M)  
Water (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58232-4029-21 in 1 CARTON
1113 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 FINALpart34810/25/201010/30/2017
Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 10/2015
Document Id: 1502fd0d-0ffc-45f5-8833-64fda88c44bf
Set id: 4a8a30b3-343c-4b36-8213-b921fc3dfd95
Version: 2
Effective Time: 20151001
 
Johnson & Johnson Consumer Inc.