BENADRYL EXTRA STRENGTH ITCH RELIEF- diphenhydramine hydrochloride and zinc acetate solution 
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.

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Benadryl Extra Strength Itch Relief Stick

Drug Facts

Active ingredientsPurpose
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
  • hold stick straight down over affected skin area
  • press tip of stick repeatedly on affected skin area until liquid flows, then dab sparingly
  • adults and children 2 years of age and older: apply to 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, povidone, purified water, tromethamine

Questions?

call 1-800-524-2624 (English/Spanish)

Dist: Johnson & Johnson
Consumer Products Company

Division of Johnson & Johnson
Consumer Companies Inc.
Skillman, NJ 08558 USA

PRINCIPAL DISPLAY PANEL - 14 mL Applicator Carton

EXTRA STRENGTH
Benadryl ®
Topical Analgesic/Skin Protectant

ITCH
RELIEF
STICK

Apply
directly
to insect
bites

Starts working
on contact

Relieves itch
and pain

For adults
and kids 2+

Insect
Bites

Mosquito
Bites

0.47 FL OZ (14 mL)

Principal Display Panel - 14 mL Applicator Carton
BENADRYL EXTRA STRENGTH ITCH RELIEF 
diphenhydramine hydrochloride and zinc acetate solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58232-0742
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:58232-0742-61 in 1 CARTON04/01/201202/21/2023
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 finalpart34704/01/201202/21/2023
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 1/2023
 
Johnson & Johnson Consumer Inc.