DrugCite

BENADRYL ORIGINAL STRENGTH  ITCH STOPPING - diphenhydramine hydrochloride and zinc acetate cream 
Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.

Original Strength
BENADRYL® ITCH STOPPING CREAM

Drug Facts

Active ingredients Purpose
Diphenhydramine hydrochloride 1% 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

  • store at 20° to 25° C (68° to 77° F)

Inactive ingredients

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

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 - 28.3g Tube Carton

ORIGINAL STRENGTH

Benadryl®
Topical Analgesic/Skin Protectant

For ages 2 & up

ITCH
STOPPING
CREAM

NET WT 1 OZ (28.3g)

PRINCIPAL DISPLAY PANEL - 28.3g Tube Carton

BENADRYL ORIGINAL STRENGTH   ITCH STOPPING
diphenhydramine hydrochloride and zinc acetate  cream
Product Information
Product Type HUMAN OTC DRUG NDC Product Code (Source) 58232-0740
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Diphenhydramine Hydrochloride (Diphenhydramine) Diphenhydramine Hydrochloride 10 mg  in 1 g
Zinc Acetate (Zinc Cation) Zinc Acetate 1 mg  in 1 g
Inactive Ingredients
Ingredient Name Strength
Cetyl Alcohol  
Diazolidinyl Urea  
Methylparaben  
Propylene Glycol  
Propylparaben  
Water  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 58232-0740-1 1  In 1 CARTON contains a TUBE
1 28.3 g In 1 TUBE This package is contained within the CARTON (58232-0740-1)

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH NOT FINAL part348 10/15/2012

Labeler - Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. (830803164)
Revised: 10/2012Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.