WAL-DRYL- diphenhydramine hydrochloride and zinc acetate cream 
Walgreen Company

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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Allergy Cream with Zinc Acetate

ACTIVE INGREDIENT

Diphenhydramine hydrochloride, USP 2%

Zinc acetate, USP 0.1%

PURPOSE

Topical analgesic

Skin protectant

USES

For the temporary relief of pain and itching associated with

WARNINGS

For external use only

DO NOT USE

ASK A DOCTOR BEFORE USE

WHEN USING THIS PRODUCT

STOP USE AND ASK A DOCTOR IF

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS

OTHER INFORMATION

INACTIVE INGREDIENT

cetyl alcohol, methylparaben, polysorbate 60, propylene glycol, purified water, sorbitan monostearate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 0363-0525-56

Walgreens  The Brand America Trusts®

Compare to the active ingredients inBENADRYL® EXTRA STRENGTH ITCH STOPPING CREAM*

Wal-dryl

Topical Analgesic/Skin Protectant

ITCH RELIEF

MAXIMUM STRENGTH

2% Diphenhydramine Hydrochloride, USP and 0.1% Zinc Acetate, USP

Temporary Relief of Itch and Pain due to

• Insect Bites • Minor Skin Irritations •Rashes from Poison Ivy, Poison Oak or Poison Sumac

PHARMACIST RECOMMENDED

NET WT. 1 OZ (28 g)

05250111F1  VC110348

*This product is not affiliated with, manufactured by, or produced by the makers or owners of Benadryl®.

Made in USA

Distributed by: Walgreen Co.,

200 Wilmot Rd., Deerfield, IL 60015-4616

Quality Guaranteed

100% Satisfaction Guaranteed with all Walgreens Products or Your Money Back. www.walgreeens.com

Wal-Dryl
WAL-DRYL 
diphenhydramine hydrochloride and zinc acetate cream
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0122
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE 2 mg  in 1 g
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 0.1 mg  in 1 g
Inactive Ingredients
Ingredient Name Strength
CARBOMER 940 (UNII: 4Q93RCW27E)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
GLYCERIN (UNII: PDC6A3C0OX)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
PARAFFIN (UNII: I9O0E3H2ZE)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
POLYSORBATE 60 (UNII: CAL22UVI4M)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0363-0122-01 1 in 1 CARTON
1 28 g in 1 TUBE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH NOT FINAL part348 03/27/2014
Labeler - Walgreen Company (008965063)
Registrant - NeoPharm Co., Ltd. (631101883)
Establishment
Name Address ID/FEI Business Operations
NeoPharm Co., Ltd. 631101883 manufacture(0363-0122)

Revised: 3/2014
Document Id: 122909d9-119e-43fe-ad8a-8c8e665eb17a
Set id: 9575213f-64ca-47ac-b2bd-01f973af910b
Version: 1
Effective Time: 20140327
 
Walgreen Company