SLEEP AID- diphenhydramine hcl solution

Sleep Aid by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active ingredient (in each 30 mL)

Diphenhydramine HCl 50 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

• a breathing problem such as emphysema or chronic bronchitis
• glaucoma
• 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 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
• mL = milliliter
• only use the dose cup provided
• take only one dose per day (24 hours)
• adults and children 12 years and over: take 30 mL at bedtime if needed or as directed by a doctor
• children under 12 years: do not use

Other information

• each 30 mL contains: sodium 11 mg
• store at 25°C (77°F); excursions permitted between 15°-30°C (59°-86°F)
• use by expiration date on package

Inactive ingredients

anhydrous citric acid, FD&C blue #1, FD&C red #40, flavor, glycerin, high fructose corn syrup, propylene glycol, purified water, sodium benzoate, sodium chloride, sodium citrate dihydrate, sucralose, sucrose, xanthan gum

Questions or comments?

1-800-426-9391

Principal display panel

 Walgreens

WALGREENS
PHARMACIST RECOMMENDED†

Compare to the active ingredient in
Vicks® ZzzQuil® Nighttime Sleep-Aid††

Sleep
Aid
DIPHENHYDRAMINE HCl 50 mg PER 30 mL /
NIGHTTIME SLEEP AID

Nighttime

Non-habit forming

AGES
12
YEARS &
OVER

6 FL OZ (177 mL)

Berry
flavor

NOT FOR TREATING PAIN, COLD OR FLU

TAMPER EVIDENT: DO NOT USE IF PRINTED
NECK WRAP IS BROKEN OR MISSING

†Our pharmacists recommend the Walgreens brand.
  We invite you to compare to national brands.

††This product is not manufactured or distributed by
The Procter & Gamble Company, owner of the registered
trademarks Vicks® and ZzzQuil®.

DISTRIBUTED BY: WALGREEN CO., DEERFIELD, IL 60015
100% SATISFACTION GUARANTEED
walgreens.com ©2026 Walgreen Co.

50844     ORG022600245

NDC: 0363-8020-45

Walgreens 44-002A

INGREDIENTS AND APPEARANCE

SLEEP AID 
diphenhydramine hcl solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-8020
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M)	DIPHENHYDRAMINE HYDROCHLORIDE	50 mg  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C RED NO. 40 (UNII: WZB9127XOA)
GLYCERIN (UNII: PDC6A3C0OX)
HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)
SUCRALOSE (UNII: 96K6UQ3ZD4)
SUCROSE (UNII: C151H8M554)
XANTHAN GUM (UNII: TTV12P4NEE)

Product Characteristics
Color	purple	Score
Shape		Size
Flavor	BERRY	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-8020-45	177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/10/2022
2	NDC: 0363-8020-02	355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/10/2022
3	NDC: 0363-8020-97	2 in 1 CARTON	03/10/2022
3		355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
4	NDC: 0363-8020-96	2 in 1 PACKAGE	03/10/2022	07/31/2026
4		355 mL in 1 BOTTLE, PLASTIC; 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	03/10/2022

Labeler - Walgreen Company (008965063)

Establishment
Name	Address	ID/FEI	Business Operations
LNK International, Inc.		967626305	manufacture(0363-8020) , pack(0363-8020)