Skip to Content

← See all Benadryl Extra Strength Itch Stopping brands

Benadryl Extra Strength Itch Stopping

Medically reviewed on August 27, 2018

Dosage form: cream
Ingredients: Diphenhydramine Hydrochloride 20mg in 1g, Zinc Acetate 1mg in 1g
Labeler: Johnson & Johnson Consumer Inc.
NDC Code: 58232-0741

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.

Extra Strength
BENADRYL ITCH STOPPING CREAM

Drug Facts

Active ingredientsPurpose
Diphenhydramine hydrochloride 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.

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: apply to affected area not more than 3 to 4 times daily
  • children under 2 years of age: ask a doctor

Other information
  • protect from excessive heat (40°C/104°F)

Inactive ingredients

cetyl alcohol, diazolidinyl urea, methylparaben, polyethylene glycol monostearate 1000, propylene glycol, propylparaben, purified water

Questions?

call toll-free 800-524-2624 (English/Spanish) or 215-273-8755 (collect)

Dist: Johnson & Johnson Consumer Products Company
Division of Johnson & Johnson Consumer Companies Inc.
Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 28.3g Tube Carton

EXTRA STRENGTH

Benadryl®

Topical Analgesic/Skin Protectant

ITCH
STOPPING
CREAM

NET WT 1 OZ (28.3g)

BENADRYL EXTRA STRENGTH   ITCH STOPPING
diphenhydramine hydrochloride and zinc acetate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58232-0741
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Diphenhydramine Hydrochloride (Diphenhydramine) Diphenhydramine Hydrochloride20 mg  in 1 g
Zinc Acetate (Zinc Cation) Zinc Acetate1 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
Cetyl Alcohol 
Diazolidinyl Urea 
Methylparaben 
Propylene Glycol 
Propylparaben 
Water 
Packaging
#Item CodePackage Description
1NDC:58232-0741-11 TUBE in 1 CARTON
128.3 g in 1 TUBE
2NDC:58232-0741-21 TUBE in 1 CARTON
236.9 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34810/15/201209/01/2018
Labeler - Johnson & Johnson Consumer Inc. (002347102)

 
Johnson & Johnson Consumer Inc.

← See all Benadryl Extra Strength Itch Stopping brands

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Hide