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

----------

Walgreens 44-329-Wal-Dryl-Delisted

Active ingredient (in each tablet)

Diphenhydramine HCl 25 mg

Purpose

Antihistamine

Uses

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

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

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

44-329

WAL-DRYL ALLERGY 
diphenhydramine hcl tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0329
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE25 mg
Inactive Ingredients
Ingredient NameStrength
STARCH, CORN (UNII: O8232NY3SJ)  
D&C RED NO. 27 ALUMINUM LAKE (UNII: ZK64F7XSTX)  
ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TALC (UNII: 7SEV7J4R1U)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
ColorpinkScoreno score
ShapeOVALSize11mm
FlavorImprint Code 44;329
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-0329-082 in 1 CARTON03/02/199008/08/2025
112 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:0363-0329-121 in 1 CARTON03/02/199008/08/2025
2100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3NDC:0363-0329-224 in 1 CARTON03/02/199008/08/2025
312 in 1 BLISTER PACK; Type 0: Not a Combination Product
4NDC:0363-0329-51365 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/02/199008/08/2025
5NDC:0363-0329-78600 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/02/199008/08/2025
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01203/02/199008/08/2025
Labeler - Walgreen Company (008965063)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.038154464pack(0363-0329)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867837manufacture(0363-0329) , pack(0363-0329)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867894manufacture(0363-0329)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.868734088manufacture(0363-0329)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.967626305pack(0363-0329)

Revised: 10/2023
Document Id: a16d3a49-51e8-457d-9614-4ef71665b886
Set id: d7c2b151-f01c-4a06-b0ad-0d940de4122f
Version: 21
Effective Time: 20231023
 
Walgreen Company