BENGAY ULTRA STRENGTH REGULAR SIZE- , unspecified form patch 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® ULTRA STRENGTH PAIN RELIEVING PATCH Regular Size Drug Facts

Active ingredient Menthol 5%

Purpose Topical

Uses temporarily relieves 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 of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions open pouch and remove patch if desired, cut patch to size peel off protective backing and apply sticky side to affected area 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 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 - 5 Patch Pouch Carton ULTRA STRENGTH MENTHOL 5% TOPICAL ANALGESIC PATCH BENGAY® PAIN RELIEVING PATCH Targeted relief that's designed to stay in place 5 INDIVIDUALLY SEALED PATCHES 3.9 IN x 5.5 IN (10 cm x 14 cm) 5 REGULAR FOR NECK TO ARM

BENGAY ULTRA STRENGTH REGULAR SIZE menthol, unspecified form patch Product Information Product T ype HUMAN OTC DRUG Ite m Code (Source ) NDC:6 9 9 6 8 -0 59 6 Route of Administration TOPICAL

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Mentho l, unspecified fo rm (UNII: L7T10 EIP3A) (Mentho l, unspecified fo rm - Mentho l, unspecified 50 mg UNII:L7T10 EIP3A) fo rm

Inactive Ingredients Ingredient Name Strength Ka o lin (UNII: 24H4NWX5CO) Ca rbo xymethylcellulo se So dium, Unspecified Fo rm (UNII: K6 79 OBS311) Glycerin (UNII: PDC6 A3C0 OX) Methylpa ra ben (UNII: A2I8 C7HI9 T) Po lya crylic Acid (8 0 0 0 MW) (UNII: 738 6 1X4K5F) Po lyso rba te 8 0 (UNII: 6 OZP39 ZG8 H) Pro pylpa ra ben (UNII: Z8 IX2SC1OH) Silico n Dio xide (UNII: ETJ7Z6 XBU4) So dium Po lya cryla te (8 0 0 0 MW) (UNII: 28 5CYO341L) So rbita n Mo no o lea te (UNII: 0 6 XEA2VD56 ) So rbito l (UNII: 50 6 T6 0 A25R) Ta rta ric Acid (UNII: W48 8 8 I119 H) Tita nium Dio xide (UNII: 15FIX9 V2JP) Wa ter (UNII: 0 59 QF0 KO0 R)

Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:6 9 9 6 8 -0 59 6 -5 5 in 1 CARTON 0 9 /0 1/20 19 1 1 in 1 POUCH; Type 0 : No t a Co mbinatio n Pro duct

Marketing Information Marke ting Cate gory Application Numbe r or Monograph Citation Marke ting Start Date Marke ting End Date OTC MONOGRAPH NOT FINAL part348 0 9 /0 1/20 19

Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 8/2020 Johnson & Johnson Consumer Inc.