Sleep Aid by WALMART INC. / LNK International, Inc. Equate 44-727-Delisted

Sleep Aid by

Drug Labeling and Warnings

Sleep Aid by is a Otc medication manufactured, distributed, or labeled by WALMART INC., LNK International, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SLEEP AID NIGHTTIME- diphenhydramine hcl capsule, liquid filled 
WALMART INC.

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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Equate 44-727-Delisted

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

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

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

Inactive Ingredients
Ingredient Name	Strength
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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79903-023-08	2 in 1 CARTON	10/28/2020	07/10/2023
1		12 in 1 BLISTER PACK; Type 0: Not a Combination Product
2	NDC: 79903-023-02	1 in 1 CARTON	10/28/2020	07/10/2023
2		12 in 1 BLISTER PACK; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part338	10/28/2020	07/10/2023

Labeler - WALMART INC. (051957769)

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

Revised: 7/2023

Document Id: 0eb16dfd-6a8a-4de4-bcfb-c62f91a0edc7

34390-5

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

Version: 4

Effective Time: 20230710

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