WAL-DRYL ALLERGY DYE-FREE- diphenhydramine hcl capsule, liquid filled

Wal-Dryl Allergy by

Drug Labeling and Warnings

Wal-Dryl Allergy by is a Otc medication manufactured, distributed, or labeled by Walgreen Company, LNK International, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (in each liquid-filled capsule)

Diphenhydramine HCl 25 mg

Purpose

Antihistamine

Uses

• temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
  • runny nose
  • itchy, watery eyes
  • sneezing
  • itching of the nose or throat
• temporarily relieves these symptoms due to the common cold:
  • runny nose
  • sneezing

Warnings

Do not use

• to make a child sleepy
• with any other product containing diphenhydramine, even one used on skin

Ask a doctor before use if you have

• a breathing problem such as emphysema or chronic bronchitis
• glaucoma
• difficulty in urination due to enlargement of the prostate gland

Ask a doctor or pharmacist before use if you are

taking sedatives or tranquilizers.

When using this product

• marked drowsiness may occur
• avoid alcoholic beverages
• alcohol, sedatives, and tranquilizers may increase drowsiness
• excitability may occur, especially in children
• use caution when driving a motor vehicle or operating machinery

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

• take every 4 to 6 hours
• do not take more than 6 doses in 24 hours

• adults and children 12 years and over: 1 to 2 capsules
• children 6 to under 12 years: 1 capsule
• children under 6 years: do not use

Other information

• TAMPER EVIDENT: DO NOT USE IF OUTER PACKAGE IS OPENED OR BLISTER IS TORN OR BROKEN
• store at 25°C (77°F); excursions permitted between 15°-30°C (59°-86°F)
• protect from heat, humidity and light
• see end flap for expiration date and lot number

Inactive ingredients

edible white ink, gelatin, glycerin, polyethylene glycol, purified water, sorbitol

Questions or comments?

1-800-426-9391

Principal display panel

Walgreens

Compare to Benadryl®
Dye-Free Allergy
active ingredient††

NDC: 0363-6580-08

Dye-Free
Wal-Dryl®

ALLERGY

DIPHENHYDRAMINE HCI 25 mg / ANTIHIS TAMINE

DYE FREE    LIQUID CAPS

Relief of runny nose, sneezing,
itchy throat & itchy, watery eyes

24
LIQUID
CAPS

ACTUAL SIZE

TAMPER EVIDENT: DO NOT USE IF PACKAGE IS OPENED OR IF
BLISTER UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF
TAMPERING

WALGREENS
PHARMACIST
RECOMMENDED†

Health expertise
you rely on.™

†Walgreens Pharmacist Survey
††This product is not manufactured or distributed by
Johnson & Johnson Corporation, owner of the registered
trademark Benadryl® Dye-Free Allergy.

50844       REV0419B65808

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

Walgreens
100%
SATISFACTION
GUARANTEED
walgreens.com   ©2018 Walgreen Co.

PRODUCT OF CHINA PACKAGED AND
QUALITY ASSURED IN THE U.S.A.

Walgreen 44-658

INGREDIENTS AND APPEARANCE

WAL-DRYL ALLERGY  DYE-FREE
diphenhydramine hcl capsule, liquid filled

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-6580
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M)	DIPHENHYDRAMINE HYDROCHLORIDE	25 mg

Inactive Ingredients
Ingredient Name	Strength
GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
GLYCERIN (UNII: PDC6A3C0OX)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
WATER (UNII: 059QF0KO0R)
SORBITOL (UNII: 506T60A25R)

Product Characteristics
Color	YELLOW (clear natural)	Score	no score
Shape	OVAL	Size	15mm
Flavor		Imprint Code	658
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-6580-08	2 in 1 CARTON	03/01/2015
1		12 in 1 BLISTER PACK; Type 0: Not a Combination Product
2	NDC: 0363-6580-22	4 in 1 CARTON	03/01/2015
2		12 in 1 BLISTER PACK; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part341	03/01/2015

Labeler - Walgreen Company (008965063)

Establishment
Name	Address	ID/FEI	Business Operations
LNK International, Inc.		832867837	PACK(0363-6580)