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NDC 00363-0190-78 Wal-Dryl 25 mg/1 Details

Wal-Dryl 25 mg/1

Wal-Dryl is a ORAL CAPSULE in the HUMAN OTC DRUG category. It is labeled and distributed by Walgreen Company. The primary component is DIPHENHYDRAMINE HYDROCHLORIDE.

MedlinePlus Drug Summary

Diphenhydramine is used to relieve red, irritated, itchy, watery eyes; sneezing; and runny nose caused by hay fever, allergies, or the common cold. Diphenhydramine is also used to relieve cough caused by minor throat or airway irritation. Diphenhydramine is also used to prevent and treat motion sickness, and to treat insomnia (difficulty falling asleep or staying asleep). Diphenhydramine is also used to control abnormal movements in people who have early stage parkinsonian syndrome (a disorder of the nervous system that causes difficulties with movement, muscle control, and balance) or who are experiencing movement problems as a side effect of a medication. Diphenhydramine will relieve the symptoms of these conditions but will not treat the cause of the symptoms or speed recovery. Diphenhydramine should not be used to cause sleepiness in children. Diphenhydramine is in a class of medications called antihistamines. It works by blocking the action of histamine, a substance in the body that causes allergic symptoms.

Related Packages: 00363-0190-78
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Diphenhydramine

Product Information

NDC	00363-0190
Product ID	0363-0190_1c97e18c-8088-4082-ba8d-153c24126b03
Associated GPIs
GCN Sequence Number	048775
GCN Sequence Number Description	nicotine polacrilex LOZENGE 4 MG BUCCAL
HIC3	J3A
HIC3 Description	SMOKING DETERRENT AGENTS (GANGLIONIC STIM,OTHERS)
GCN	14688
HICL Sequence Number	002049
HICL Sequence Number Description	NICOTINE POLACRILEX
Brand/Generic	Generic
Proprietary Name	Wal-Dryl
Proprietary Name Suffix	n/a
Non-Proprietary Name	Diphenhydramine HCl
Product Type	HUMAN OTC DRUG
Dosage Form	CAPSULE
Route	ORAL
Active Ingredient Strength	25
Active Ingredient Units	mg/1
Substance Name	DIPHENHYDRAMINE HYDROCHLORIDE
Labeler Name	Walgreen Company
Pharmaceutical Class	Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	part341
Listing Certified Through	n/a

Package

Package Images

NDC 00363-0190-78 (00363019078)

Pricing Information	N/A
NDC Package Code	0363-0190-78
Billing NDC	00363019078
Package	600 CAPSULE in 1 BOTTLE, PLASTIC (0363-0190-78)
Marketing Start Date	1990-03-15
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 58b6ac64-fc09-4bb8-a6ed-97875c5ee11a Details

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 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 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

GUARANTEED

walgreens.com

©2018 Walgreen Co.

Walgreens 44-190

INGREDIENTS AND APPEARANCE

WAL-DRYL

diphenhydramine hcl capsule

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0363-0190
Route of Administration	ORAL

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

Ingredient Name	Strength
Inactive Ingredients
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
Color	pink, white	Score	no score
Shape	CAPSULE	Size	14mm
Flavor		Imprint Code	44;107
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0363-0190-08	2 in 1 CARTON	03/15/1990	03/22/2024
1		12 in 1 BLISTER PACK; Type 0: Not a Combination Product
2	NDC:0363-0190-51	365 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/15/1990	03/22/2024
3	NDC:0363-0190-78	600 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/15/1990	03/22/2024
4	NDC:0363-0190-07	3 in 1 CARTON	03/15/1990	08/14/2022
4		12 in 1 BLISTER PACK; Type 0: Not a Combination Product
5	NDC:0363-0190-22	4 in 1 CARTON	03/15/1990	07/23/2021
5		12 in 1 BLISTER PACK; Type 0: Not a Combination Product
6	NDC:0363-0190-23	6 in 1 CARTON	03/15/1990	03/05/2022
6		12 in 1 BLISTER PACK; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part341	03/15/1990	03/22/2024

Labeler - Walgreen Company (008965063)

Name	Address	ID/FEI	Business Operations
Establishment
LNK International, Inc.		038154464	pack(0363-0190)

Name	Address	ID/FEI	Business Operations
Establishment
LNK International, Inc.		832867837	pack(0363-0190)

Name	Address	ID/FEI	Business Operations
Establishment
LNK International, Inc.		868734088	manufacture(0363-0190) , pack(0363-0190)

Name	Address	ID/FEI	Business Operations
Establishment
LNK International, Inc.		967626305	pack(0363-0190)

Revised: 6/2022

Document Id: 1c97e18c-8088-4082-ba8d-153c24126b03

Set id: 58b6ac64-fc09-4bb8-a6ed-97875c5ee11a

Version: 24

Effective Time: 20220607