BENADRYL EXTRA STRENGTH ITCH RELIEF- diphenhydramine hydrochloride and zinc acetate solution 
Johnson & Johnson Consumer Inc.

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Benadryl ® EXTRA STRENGTH ITCH RELIEF STICK

Drug Facts

Active ingredientPurpose
Diphenhydramine HCl 2%Topical analgesic
Zinc acetate 0.1%Skin protectant

Uses

Warnings

For external use only.

Flammable. Keep away from fire or flame.

Do not use

  • on large areas of the body
  • with any other product containing diphenhydramine, even one taken by mouth

Ask a doctor before use

  • on chicken pox
  • on measles

When using this product avoid contact with eyes

Stop use and ask a doctor if

  • condition worsens or does not improve within 7 days
  • symptoms persist for more than 7 days or clear up and occur again within a few days

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

Inactive ingredients

alcohol, glycerin, PVP, purified water, tromethamine

Questions?

call 1-877-717-2824 (toll-free) or 215-273-8755 (collect) www.benadryl.com

Distributed by:
JOHNSON & JOHNSON CONSUMER INC.
Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 14 mL Applicator Carton

Benadryl ®®

Apply directly

to insect bites

EXTRA STRENGTH

For Ages 2+

ITCH

RELIEF

STICK

Diphenhydramine HCL 2% /

Topical Analgesic

Zinc acetate 0.1% /

Skin Protectant

Starts working

on contact

Relieves itch

and pain

Insect Mosquito

Bites Bites

0.47 FL OZ (14mL)

Benadryl_01

BENADRYL EXTRA STRENGTH ITCH RELIEF 
diphenhydramine hydrochloride and zinc acetate solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0459
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC ACETATE1 mg  in 1 mL
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
WATER (UNII: 059QF0KO0R)  
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
GLYCERIN (UNII: PDC6A3C0OX)  
TROMETHAMINE (UNII: 023C2WHX2V)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0459-11 in 1 CARTON06/01/2019
114 mL in 1 APPLICATOR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01706/01/2019
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 1/2024
Document Id: 0f35ee45-e226-9bc4-e063-6394a90ae9ee
Set id: 309d9be0-e367-429a-a1fa-ab7855477c8a
Version: 6
Effective Time: 20240118
 
Johnson & Johnson Consumer Inc.