WAL-DRYL- diphenhydramine hydrochloride and zinc acetate cream

Wal-dryl by

Drug Labeling and Warnings

Wal-dryl by is a Otc medication manufactured, distributed, or labeled by Walgreen Company, NeoPharm Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

• minor burns
• sunburn
• minor cuts
• scrapes
• insect bites
• minor skin irritations
• rashes due to poison ivy, oak and sumac
• dries the oozing and weeping of poison:
  • ivy
  • oak
  • 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 the eyes

STOP USE AND ASK A DOCTOR IF

• condition gets worse
• 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 often 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 between 59°-86°F (15°-30°C).

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

INGREDIENTS AND APPEARANCE

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

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)