WAL- DRYL ITCH RELIEF- diphenhydramine hydrochloride and zinc acetate cream 
WALGREENS

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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WAL- DRYL® ITCH RELIEF CREAM

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

Walgreens

Wal-Dryl®
Itch Relief Cream

DIPHENHYDRAMINE HYDROCHLORIDE
USP 1% / ANTI-ITCH CREAM

NET WT 1 OZ (28 g)

PRINCIPAL DISPLAY PANEL - 28 g Tube Carton
WAL- DRYL ITCH RELIEF 
diphenhydramine hydrochloride and zinc acetate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0121
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE10 mg  in 1 g
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC ACETATE1 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
POLYSORBATE 60 (UNII: CAL22UVI4M)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
MINERAL OIL (UNII: T5L8T28FGP)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-0121-001 in 1 CARTON12/21/2020
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 NOT FINALpart34812/21/2020
Labeler - WALGREENS (008965063)
Establishment
NameAddressID/FEIBusiness Operations
Natureplex LLC062808196MANUFACTURE(0363-0121)

Revised: 1/2021
Document Id: b5a8d82f-4f8a-43e3-b1d6-5450255930be
Set id: 6e57d9b3-1d93-41ce-8a38-af01e7da0a0f
Version: 2
Effective Time: 20210105
 
WALGREENS