Benadryl extra strength itch stopping cream

Spl unclassified section

Drug Facts

Otc - active ingredient section

Otc - purpose section

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


  • 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


Otc - do not use section

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

Otc - when using section

When using this productavoid 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

Otc - keep out of reach of children section

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


  • 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 (40C/104F)

Inactive ingredients

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


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

Spl unclassified section

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

Ingredients and appearance - Product information

Benadryl extra strength itch stopping cream- Diphenhydramine hydrochloride and zinc acetate

Product information

Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC: 58232-0741
Route of Administration Topical

Active Ingredient/Active Moiety

Ingredient Name Strength
Diphenhydramine hydrochloride ( UNII: TC2D6JAD40)( Diphenhydramine - UNII: 8GTS82S83M ) 20 mgin 1 g
Zinc acetate ( UNII: FM5526K07A)( Zinc cation - UNII: 13S1S8SF37 ) 1 mgin 1 g

Inactive Ingredients

Ingredient Name Code
Cetyl alcohol ( UNII: 936JST6JCN)
Diazolidinyl urea ( UNII: H5RIZ3MPW4)
Methylparaben ( UNII: A2I8C7HI9T)
Propylene glycol ( UNII: 6DC9Q167V3)
Propylparaben ( UNII: Z8IX2SC1OH)
Water ( UNII: 059QF0KO0R)

Product Characteristics

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
OTC monograph not final part348 USA

Labeler - Johnson & Johnson Consumer Inc.( 002347102)

Principal display panel - 28.3g tube carton


Benadryl ®

Topical Analgesic/Skin Protectant


NET WT 1 OZ (28.3g)