WAL-DRYL- diphenhydramine hcl capsule 
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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Walgreens 44-190-Delisted

Active ingredient (in each banded 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

  • glaucoma
  • a breathing problem such as emphysema or chronic bronchitis
  • 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
  • do not take more than 6 doses in 24 hours
adults and children 12 years and over1 to 2 capsules
children 6 to under 12 years1 capsule
children under 6 yearsdo not use

Other information

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

Inactive ingredients

butylparaben, corn starch, D&C red #28, edible ink, FD&C blue #1, FD&C red #40, gelatin, lactose anhydrous, magnesium stearate, methylparaben, polysorbate 80, propylparaben, silicon dioxide

Questions or comments?

1-800-426-9391

Principal Display Panel

Walgreens

Compare to Benadryl®
Allergy active ingredient††

NDC 0363-0190-08

Wal-Dryl®

ALLERGY
DIPHENHYDRAMINE HCl 25 mg / ANTIHISTAMINE

CAPSULES

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

24 CAPSULES

ACTUAL SIZE

TAMPER EVIDENT: DO NOT USE IF PACKAGE IS OPENED
OR IF BLISTER UNIT IS TORN OR BROKEN OR IF
RED BAND AROUND CAPSULE IS BROKEN OR MISSING

DOES NOT CONTAIN GLUTEN

Walgreens
Trusted since 1901™
PHARMACIST
RECOMMENDED

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

50844     ORG111719008

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

Walgreens 44-190

Walgreens 44-190

WAL-DRYL 
diphenhydramine hcl capsule
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0190
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
BUTYLPARABEN (UNII: 3QPI1U3FV8)  
STARCH, CORN (UNII: O8232NY3SJ)  
D&C RED NO. 28 (UNII: 767IP0Y5NH)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GELATIN, UNSPECIFIED (UNII: 2G86QN327L)  
ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
Product Characteristics
Colorpink, whiteScoreno score
ShapeCAPSULESize14mm
FlavorImprint Code 44;107
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-0190-082 in 1 CARTON03/15/199003/22/2024
112 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:0363-0190-51365 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/15/199003/22/2024
3NDC:0363-0190-78600 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/15/199003/22/2024
4NDC:0363-0190-073 in 1 CARTON03/15/199008/14/2022
412 in 1 BLISTER PACK; Type 0: Not a Combination Product
5NDC:0363-0190-224 in 1 CARTON03/15/199007/23/2021
512 in 1 BLISTER PACK; Type 0: Not a Combination Product
6NDC:0363-0190-236 in 1 CARTON03/15/199003/05/2022
612 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34103/15/199003/22/2024
Labeler - Walgreen Company (008965063)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.038154464pack(0363-0190)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867837pack(0363-0190)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.868734088manufacture(0363-0190) , pack(0363-0190)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.967626305pack(0363-0190)

Revised: 6/2022
 
Walgreen Company