OTC Medication Information: WAL-DRYL ALLERGY

WAL-DRYL ALLERGY- diphenhydramine hydrochloride tablet, film coated
Walgreen Company

Active ingredient (in each tablet)

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
  • use caution when driving a motor vehicle or operating machinery
  • excitability may occur, especially in children

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, or as directed by a doctor
  • do not take more than 6 times in 24 hours
adults and children 12 years and over 1 to 2 tablets
children 6 to under 12 years 1 tablet
children under 6 years do not use

Other information

  • each tablet contains: calcium 30 mg
  • TAMPER EVIDENT: DO NOT USE IF OUTER PACKAGE IS OPENED OR BLISTER IS TORN OR BROKEN
  • store at 25ºC (77ºF); excursions permitted between 15º-30ºC (59º-86ºF)

  • protect from moisture
  • see end flap for expiration date and lot number

Inactive ingredients

corn starch, D&C red #27 aluminum lake, dicalcium phosphate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, silicon dioxide, stearic acid, talc, titanium dioxide

Questions or comments?

1-800-426-9391

Principal Display Panel

Walgreens

NDC 0363-0329-08

Compare to Benadryl®
Allergy Ultratab® Tablets
active ingredient††

Wal-Dryl®
ALLERGY

DIPHENHYDRAMINE HCl 25 mg / ANTIHISTAMINE

MINI TABS

• Relief of runny nose, sneezing,
itchy throat & itchy, watery eyes
• Easy-to-swallow mini tabs

24
COATED
MINI TABS

Actual Size

NOT FOR HOUSEHOLDS WITH YOUNG CHILDREN

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

DOES NOT CONTAIN GLUTEN

Walgreens Pharmacist Survey
Walgreens PHARMACIST RECOMMENDED

Trusted since 1901TM

Health expertise
you rely on.TM

†† This product is not manufactured or distributed
by Johnson & Johnson Corporation, owner of
the registered trademark Benadryl® Allergy
Ultratab® Tablets.

DISTRIBUTED BY: WALGREEN CO.
200 WILMOT RD., DEERFIELD, IL 60015
100% SATISFACTION GUARANTEED walgreens.com ©2018 Walgreen Co.

50844 REV1016A32908

44-329
(click image for full-size original)

44-329

WAL-DRYL ALLERGY diphenhydramine hcl tablet, film coated
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0329
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DIPHENHYDRAMINE HYDROCHLORIDE (DIPHENHYDRAMINE) DIPHENHYDRAMINE HYDROCHLORIDE 25 mg
Inactive Ingredients
Ingredient Name Strength
STARCH, CORN
D&C RED NO. 27 ALUMINUM LAKE
ANHYDROUS DIBASIC CALCIUM PHOSPHATE
MAGNESIUM STEARATE
MICROCRYSTALLINE CELLULOSE
POLYETHYLENE GLYCOL, UNSPECIFIED
POLYVINYL ALCOHOL, UNSPECIFIED
SILICON DIOXIDE
STEARIC ACID
TALC
TITANIUM DIOXIDE
Product Characteristics
Color pink Score no score
Shape OVAL Size 11mm
Flavor Imprint Code 44;329
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0363-0329-08 2 BLISTER PACK in 1 CARTON contains a BLISTER PACK
1 12 TABLET, FILM COATED in 1 BLISTER PACK This package is contained within the CARTON (0363-0329-08)
2 NDC:0363-0329-12 1 BOTTLE, PLASTIC in 1 CARTON contains a BOTTLE, PLASTIC
2 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC This package is contained within the CARTON (0363-0329-12)
3 NDC:0363-0329-22 4 BLISTER PACK in 1 CARTON contains a BLISTER PACK
3 12 TABLET, FILM COATED in 1 BLISTER PACK This package is contained within the CARTON (0363-0329-22)
4 NDC:0363-0329-51 365 TABLET, FILM COATED in 1 BOTTLE, PLASTIC None
5 NDC:0363-0329-78 600 TABLET, FILM COATED in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC Monograph Drug M012 03/02/1990 08/08/2025
Labeler — Walgreen Company (008965063)
Establishment
Name Address ID/FEI Operations
LNK International, Inc. 038154464 pack (0363-0329)
Establishment
Name Address ID/FEI Operations
LNK International, Inc. 832867837 manufacture (0363-0329), pack (0363-0329)
Establishment
Name Address ID/FEI Operations
LNK International, Inc. 832867894 manufacture (0363-0329)
Establishment
Name Address ID/FEI Operations
LNK International, Inc. 868734088 manufacture (0363-0329)
Establishment
Name Address ID/FEI Operations
LNK International, Inc. 967626305 pack (0363-0329)

Revised: 10/2023 Walgreen Company

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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