BENGAY ULTRA STRENGTH PAIN RELIEVING  LARGE SIZE - menthol patch 
Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, 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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Drug Facts

Active ingredient

Menthol 5%

Purpose

Topical analgesic

Uses

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

Other Information

Inactive ingredients

carboxymethylcellulose sodium, glycerin, kaolin, methyl acrylate/2-ethylhexyl acrylate copolymer, polyacrylic acid, polysorbate 80, sodium polyacrylate, tartaric acid, titanium dioxide, and water

Questions?

call 1-800-223-0182

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

PRINCIPAL DISPLAY PANEL - 4 Pouch Carton

ULTRA STRENGTH
BENGAY®
PAIN RELIEVING PATCH

Menthol Topical Analgesic Patch

LARGE SIZE
Good for Back to Hip

4 INDIVIDUALLY SEALED PATCHES
3.9 in × 7.9 in (10 cm × 20 cm)

PRINCIPAL DISPLAY PANEL - 4 Pouch Carton

BENGAY ULTRA STRENGTH PAIN RELIEVING   LARGE SIZE
menthol patch
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:58232-4025
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Menthol (Menthol) Menthol 50 mg
Inactive Ingredients
Ingredient Name Strength
Carboxymethylcellulose sodium  
Glycerin  
Kaolin  
Polysorbate 80  
Tartaric Acid  
Titanium Dioxide  
Water  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:58232-4025-4 4 POUCH ( POUCH) in 1 CARTON contains a POUCH
1 1 PATCH ( PATCH) in 1 POUCH This package is contained within the CARTON (58232-4025-4)

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH NOT FINAL part348 09/22/2011

Labeler - Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. (830803164)

Revised: 09/2011 Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.