BENADRYL EXTRA STRENGTH ITCH COOLING- diphenhydramine hydrochloride and zinc acetate spray 
Kenvue Brands LLC

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Benadryl ® EXTRA STRENGTH ITCH COOLING SPRAY

Drug Facts

Active ingredientsPurpose
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 1-800-524-2624 (English/Spanish)

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

PRINCIPAL DISPLAY PANEL - 59 mL Bottle Label

Benadryl®

Relief for most outdoor itches

EXTRA STRENGTH

ITCH COOLING SPRAY

Diphenhydramine HCl 2% / Topical Analgesic

Zinc acetate 0.1 % / Skin Protectant

Questions?

call 1-877-717-2824 (toll-free)

or 215-273-8755 (collect)

www.benadryl.com

Insect

Bites
Poison Ivy,

Oak, Sumac
Mosquito

Bites
SunburnMinor Cuts

& Scrapes

Distributed by:

JOHNSON & JOHNSON

CONSUMER INC.

Skillman, NJ 08558

J&JCI 2023 Made in Canada

Pat.www.jjcipats.com

2 FL OZ (59 mL)

Benadryl_01

BENADRYL EXTRA STRENGTH ITCH COOLING 
diphenhydramine hydrochloride and zinc acetate spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0270
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE20 mg  in 1 mL
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC ACETATE1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
GLYCERIN (UNII: PDC6A3C0OX)  
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
WATER (UNII: 059QF0KO0R)  
TROMETHAMINE (UNII: 023C2WHX2V)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0270-259 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product04/01/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01704/01/2019
Labeler - Kenvue Brands LLC (118772437)

Revised: 11/2024
Document Id: 21c35b88-b0f9-740e-e063-6294a90a0f1a
Set id: a7eae5dc-9db6-4bdf-9179-76060e75e044
Version: 6
Effective Time: 20241106
 
Kenvue Brands LLC