Drug Facts

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

Uses

temporarily relieves pain and itching associated with:
- insect bites
- minor burns
- sunburn
- minor skin irritations
- minor cuts
- scrapes
- rashes due to poison ivy, poison oak, and poison sumac
- dries the oozing and weeping of poison ivy, poison oak and poison sumac

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

do not use more than directed
adults and children 2 years of age and older: spray on affected area not more than 3 to 4 times daily
children under 2 years of age: ask a doctor

Other information

store at 20° to 25° C (68° to 77° F)

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

Sunburn

Minor 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 Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69968-0270
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M)	DIPHENHYDRAMINE HYDROCHLORIDE	20 mg in 1 mL
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37)	ZINC ACETATE	1 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
GLYCERIN (UNII: PDC6A3C0OX)
ALCOHOL (UNII: 3K9958V90M)
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
WATER (UNII: 059QF0KO0R)
TROMETHAMINE (UNII: 023C2WHX2V)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:69968-0270-2	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/01/2019

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M017	04/01/2019

Labeler - Johnson & Johnson Consumer Inc. (118772437)

Benadryl ® EXTRA STRENGTH ITCH COOLING SPRAY

Uses

Warnings

Do not use

Ask a doctor before use

Stop use and ask a doctor if

Directions

Other information

Inactive ingredients

Questions?

PRINCIPAL DISPLAY PANEL - 59 mL Bottle Label