BENGAY ULTRA STRENGTH LARGE SIZE- menthol, unspecified form patch 
Johnson & Johnson Consumer Inc.

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BENGAY ® ULTRA STRENGTH PAIN RELIEVING PATCH

Large Size

Drug Facts

Active ingredient

Menthol 5%

Purpose

Topical analgesic

Uses

temporarily relieves 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

Inactive ingredients

calcined kaolin, cellulose gum, glycerin, methyl acrylate/2-ethylhexyl acrylate copolymer, methylparaben, polyacrylic acid, polysorbate 80, propylparaben, silica, sodium polyacrylate, sodium polyacrylate starch, sorbitan oleate, sorbitol, tartaric acid, titanium dioxide, 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 - 4 Patch Pouch Carton

ULTRA STRENGTH
MENTHOL 5% TOPICAL ANALGESIC PATCH
BENGAY ®

PAIN RELIEVING PATCH
Targeted relief
that's designed to
stay in place

4 INDIVIDUALLY SEALED PATCH
3.9 IN x 7.9 IN (10 cm x 20 cm)

4
LARGE

FOR BACK TO HIP

PRINCIPAL DISPLAY PANEL - 4 Patch Pouch Carton
BENGAY ULTRA STRENGTH  LARGE SIZE
menthol, unspecified form patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0487
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
Inactive Ingredients
Ingredient NameStrength
KAOLIN (UNII: 24H4NWX5CO)  
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)  
GLYCERIN (UNII: PDC6A3C0OX)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
POLYACRYLIC ACID (8000 MW) (UNII: 73861X4K5F)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)  
SORBITAN MONOOLEATE (UNII: 06XEA2VD56)  
SORBITOL (UNII: 506T60A25R)  
TARTARIC ACID (UNII: W4888I119H)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0487-11 in 1 CARTON04/03/201904/14/2024
11 in 1 POUCH; Type 0: Not a Combination Product
2NDC:69968-0487-44 in 1 CARTON09/01/2019
21 in 1 POUCH; 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: 07d3138f-5746-ad20-e063-6394a90a87ab
Set id: f57ccc33-400b-4401-a348-c54d1eb9f5d0
Version: 6
Effective Time: 20231016
 
Johnson & Johnson Consumer Inc.