WALGREENS ORIGINAL STRENGTH ANTI ITCH- diphenhydramine hydrochloride, zinc acetate cream 
Walgreen Company

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Walgreens Original Strength Anti Itch

Drug Facts

Active ingredientsPurposes
Diphenhydramine hydrochloride 1%Topical analgesic
Zinc acetate 0.1%Skin protectant

Uses

Temporarily relieves pain and itching associated with:

Dries the oozing and weeping of poison ivy, poison oak and poison sumac

Warnings

For external use only.

Avoid contact with eyes.

Do not use

  • more than directed
  • on large areas of the body
  • with any product containing diphenhydramine even one taken by mouth

Ask a doctor before use

  • on chicken pox
  • on measles

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

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away: 800-222-1222.

Directions

Other information

Inactive ingredients

cetearyl alcohol (and) polysorbate 60, DMDM hydantoin, glyceryl stearate, isopropyl myristate, methylparaben, mineral oil, propylparaben, purified water

Questions or comments?

1-866-323-0107

DISTRIBUTED BY: WALGREEN CO.
200 WILMOT RD., DEERFIELD, IL 60015

PRINCIPAL DISPLAY PANEL - 28 g Tube Carton

Itch Relief
Cream
DIPHENHYDRAMINE HYDROCHLORIDE USP 1% / ANTI-ITCH CREAM

NET WT 1 OZ (28 g)

PRINCIPAL DISPLAY PANEL - 28 g Tube Carton
WALGREENS ORIGINAL STRENGTH ANTI ITCH 
diphenhydramine hydrochloride, zinc acetate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-4115
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE1 g  in 100 g
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC ACETATE0.1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
METHYLPARABEN (UNII: A2I8C7HI9T)  
POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-4115-281 in 1 CARTON09/27/2013
128 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph drugM01709/27/2013
Labeler - Walgreen Company (008965063)
Establishment
NameAddressID/FEIBusiness Operations
Natureplex LLC062808196MANUFACTURE(0363-4115)

Revised: 9/2023
Document Id: c333512f-e44c-4caf-b675-db2ea3a93daa
Set id: a6a49dbb-74c7-47ca-88f2-3bb3d9acf914
Version: 11
Effective Time: 20230927
 
Walgreen Company