EQUATE NIGHTTIME SLEEP-AID- diphenhydramine hydrochloride capsule, liquid filled

equate NIGHTTIME Sleep-Aid by

Drug Labeling and Warnings

equate NIGHTTIME Sleep-Aid by is a Otc medication manufactured, distributed, or labeled by WALMART INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient (in each softgel)

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 
with other drugs that cause drowsiness such as antihistamines and nighttime cold/flu products

Ask a doctor before use if you have glaucoma heart diseases 
a breathing problem such as emphysema, asthma, 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, tranquilizers, or any other sleep aid

When using this product  avoid alcoholic beverages and other drugs that cause drowsiness. Be careful when driving a motor vehicle or operating machinery.

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. 
Overdose warning: In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away. Prompt medical attention is critical for adults as well as children even if you do not notice any signs or symptoms.

Directions

 take only one dose (2 softgels) per day (24 hours)

• adults and children 12 years and over: take 2 softgels at bedtime if needed ; or as directed by a doctor
• children under 12 years: do not use

Other information

protect from light, heat and moisture
store at controlled room temperature 20-25°C (68-77°F)

Inactive ingredients

FD&C Blue No. 1, FD&C Red No. 40, gelatin, glycerin, polyethylene glycol 400, sorbitol sorbitan solution, titanium dioxide

Questions or comments?

1-888-287-1915

SPL UNCLASSIFIED SECTION

Compare to Vicks® ​ZzzQuil™ NIGHTTIME SLEEP-AID LiquiCaps™ active ingredient*

 Fall asleep fast
Not for treating pain, cold or flu

READ AND KEEP OUTER CARTON FOR COMPLETE PRODUCT WARNINGS AND INFORMATION

Satisfaction GuaranteedFor more information call 1-888-287-1915 or visit Walmart.com/help

DISTRIBUTED BY: Walmart Inc.,
Bentonville, AR 72716

PRODUCT OF INDIA

*This product is not manufactured or distributed by The Procter & Gamble Co., owner of the registered trademarks Vicks®, ZzzQuil™, and LiquiCaps™.

TAMPER EVIDENT: DO NOT USE IF PACKAGE IS OPENED OR IF BLISTER UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING.

Packaging

INGREDIENTS AND APPEARANCE

EQUATE NIGHTTIME SLEEP-AID 
diphenhydramine hydrochloride capsule, liquid filled

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79903-400
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)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
SORBITOL (UNII: 506T60A25R)
SORBITAN (UNII: 6O92ICV9RU)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	purple	Score	no score
Shape	OVAL	Size	14mm
Flavor		Imprint Code	912
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79903-400-12	1 in 1 CARTON	10/21/2025
1		12 in 1 BLISTER PACK; Type 0: Not a Combination Product
2	NDC: 79903-400-24	2 in 1 CARTON	10/21/2025
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 Drug	M010	10/21/2025

Labeler - WALMART INC. (051957769)