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NDC 79903-0023-02 Sleep Aid 25 mg/1 Details

Sleep Aid 25 mg/1

Sleep Aid is a ORAL CAPSULE, LIQUID FILLED in the HUMAN OTC DRUG category. It is labeled and distributed by WALMART INC.. 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: 79903-0023-02
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Diphenhydramine

Product Information

NDC	79903-0023
Product ID	79903-023_5bc7f0d7-fbe2-4a02-a3a7-20216b26cfda
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Sleep Aid
Proprietary Name Suffix	Nighttime
Non-Proprietary Name	Diphenhydramine HCl
Product Type	HUMAN OTC DRUG
Dosage Form	CAPSULE, LIQUID FILLED
Route	ORAL
Active Ingredient Strength	25
Active Ingredient Units	mg/1
Substance Name	DIPHENHYDRAMINE HYDROCHLORIDE
Labeler Name	WALMART INC.
Pharmaceutical Class	Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	part338
Listing Certified Through	2023-12-31

Package

Package Images

NDC 79903-0023-02 (79903002302)

Pricing Information	N/A
NDC Package Code	79903-023-02
Billing NDC	79903002302
Package	1 BLISTER PACK in 1 CARTON (79903-023-02) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Marketing Start Date	2020-10-28
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL c966d9e9-8fef-4f87-b996-477c618af993 Details

Active ingredient (in each liquid-filled capsule)

Diphenhydramine HCl 25 mg

Purpose

Nighttime sleep-aid

Uses

for relief of occasional sleeplessness
reduces time to fall asleep if you have difficulty falling asleep

Warnings

Do not use

for children under 12 years of age
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

avoid alcoholic beverages.

Stop use and ask a doctor if

sleeplessness persists continuously for more than 2 weeks. Insomnia may be a symptom of a serious underlying medical illness.

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 right away.

Directions

do not take more than directed
take only one dose per day (24 hours)
adults and children 12 years and over: take 2 capsules at bedtime if needed or as directed by a doctor
children under 12 years: do not use

Other information

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

Inactive ingredients

FD&C blue #1, FD&C red #40, gelatin, glycerin, isopropyl alcohol, medium chain triglycerides, polyethylene glycol, povidone, purified water, sorbitol sorbitan solution, white ink

Questions or comments?

1-888-287-1915

Principal display panel

equate™

NDC 79903-023-08

Compare to

VICKS® ZzzQuil®

NIGHTTIME SLEEP-AID

LiquiCaps® active

ingredient*

NIGHTTIME

Sleep-Aid

Diphenhydramine HCl 25 mg

Nighttime Sleep-Aid

• Non-habit forming

• Not for treating pain, cold or flu

25

mg

EACH

24

SOFTGELS

Actual Size

TAMPER EVIDENT: DO NOT USE IF PACKAGE IS

OPENED OR IF BLISTER UNIT IS TORN, BROKEN OR

SHOWS ANY SIGNS OF TAMPERING

Satisfaction guaranteed - Or we'll replace it

or give you your money back. For questions

or comments please call 1-888-287-1915.

DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716

PRODUCT OF UNITED ARAB EMIRATES

*This product is not manufactured or distributed by The

Procter & Gamble Company, owner of the registered trademark

VICKS® ZzzQuil® NIGHTTIME SLEEP-AID LiquiCaps®.

50844 ORG012072708

Equate 44-727

INGREDIENTS AND APPEARANCE

SLEEP AID NIGHTTIME

diphenhydramine hcl capsule, liquid filled

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:79903-023
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
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C RED NO. 40 (UNII: WZB9127XOA)
GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
WATER (UNII: 059QF0KO0R)
SORBITOL (UNII: 506T60A25R)
SORBITAN (UNII: 6O92ICV9RU)

Product Characteristics
Color	purple (clear)	Score	no score
Shape	OVAL	Size	16mm
Flavor		Imprint Code	727
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:79903-023-08	2 in 1 CARTON	10/28/2020
1		12 in 1 BLISTER PACK; Type 0: Not a Combination Product
2	NDC:79903-023-02	1 in 1 CARTON	10/28/2020
2		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	part338	10/28/2020

Labeler - WALMART INC. (051957769)

Name	Address	ID/FEI	Business Operations
Establishment
LNK International, Inc.		832867837	pack(79903-023)

Revised: 10/2022

Document Id: 5bc7f0d7-fbe2-4a02-a3a7-20216b26cfda

Set id: c966d9e9-8fef-4f87-b996-477c618af993

Version: 3

Effective Time: 20221029