ANTI-ITCH- diphenhydramine hydrochloride and zinc acetate cream 
Amerisource Bergen

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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Anti-Itch Cream

Drug Facts

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

Uses

temporarily relieves pain and itching associated with:

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

Other information

Inactive ingredients

cetyl alcohol, glyceryl stearate, glyceryl stearate/PEG-100 stearate, methylparaben, propylene glycol, propylparaben and purified water

Questions?

Call 1-866-923-4914

Distributed By
AmerisourceBergen
1300 Morris Drive
Chesterbrook, PA 19087

PRINCIPAL DISPLAY PANEL - 28.4 g Tube Carton

GOOD
NEIGHBOR
PHARMACY®

Compare to Extra Strength Benadryl®
Itch Stopping Cream* active ingredients*

NDC 24385-210-03

Anti-Itch Cream
Diphenhydramine hydrochloride 2% and Zinc acetate 0.1%

Topical Analgesic • Skin Protectant

NET WT 1 oz (28.4 g)

PRINCIPAL DISPLAY PANEL - 28.4 g Tube Carton
ANTI-ITCH 
diphenhydramine hydrochloride and zinc acetate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24385-210
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Diphenhydramine hydrochloride (UNII: TC2D6JAD40) (Diphenhydramine - UNII:8GTS82S83M) Diphenhydramine hydrochloride20 mg  in 1 g
Zinc acetate (UNII: FM5526K07A) (Zinc Cation - UNII:13S1S8SF37) Zinc acetate1 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
cetyl alcohol (UNII: 936JST6JCN)  
glyceryl monostearate (UNII: 230OU9XXE4)  
methylparaben (UNII: A2I8C7HI9T)  
propylene glycol (UNII: 6DC9Q167V3)  
propylparaben (UNII: Z8IX2SC1OH)  
water (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:24385-210-031 in 1 CARTON09/20/2005
128.4 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart34809/20/2005
Labeler - Amerisource Bergen (007914906)
Registrant - Taro Pharmaceuticals U.S.A., Inc (145186370)
Establishment
NameAddressID/FEIBusiness Operations
Taro Pharmaceuticals Inc.206263295MANUFACTURE(24385-210)

Revised: 6/2020
Document Id: 78575eb6-cbf4-4967-a519-2a9983495da1
Set id: 4275c286-225d-4b03-bff0-8fca07959d7c
Version: 2
Effective Time: 20200618
 
Amerisource Bergen