FDA.reportPublic FDA data

meijer Alcohol-Free Nighttime Sleep-Aid Diphenhydramine HCl

Manufacturer
MEIJER DISTRIBUTION INC
Effective date
2026-10-05
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
daily-update
Hydrated at
2026-10-07 01:02:44

Label at a glance#

ProductMeijer Nighttime Sleep-aid Berry Flavor
Active ingredientDIPHENHYDRAMINE HYDROCHLORIDE
Label structure9 sections

Indications and uses

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

Dosage and administration

▪ take only one dose per day (24 hours) ▪ measure with dosing cup provide adults & children 12 yrs & over One Dose = 30 mL at bed time if needed or as directed by a doctor Children under 12 yrs do not use Other information • each 30 mL dose contains: sodium 23 mg • store at room temperature • protect from light. Does not meet USP requirement for light-resistant packaging.

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (In each 30 mL)

Diphenhydramine HCl 50 mg

Purpose

OTC - PURPOSE SECTION

Nighttime sleep-aid

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

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

OTC - ASK DOCTOR SECTION

  • 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 two 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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Overdose warning: In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Directions

DOSAGE & ADMINISTRATION SECTION

  • take only one dose per day (24 hours)
  • measure with dosing cup provide

adults & children 12 yrs & over

One Dose = 30 mL at bed time if needed or as directed by a doctor

Children under 12 yrs

do not use

Other information

  • each 30 mL dose contains: sodium 23 mg
  • store at room temperature
  • protect from light. Does not meet USP requirement for light-resistant packaging.

Inactive ingredients

INACTIVE INGREDIENT SECTION

anhydrous citric acid, FD&C Blue #1, FD&C Red #40, glycerin, natural and artificial flavor, potassium citrate, purified water, sodium benzoate, sorbitol, sucralose, xanthan gum.

Questions or comments?

OTC - QUESTIONS SECTION

1-866-467-2748

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL 12 FL OZ (354 mL Bottle)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

meijer®
NDC# 41250-738-12
Compare to Zzzquil® Nighttime Sleep-Aid* active ingredient*

NighttimeSleep-aid

Diphenhydramine HCl 50 mg

  • Non-Habit Forming

Alcohol-Free

Not for treating Cold or Flu, See Warnings

Berry Flavor

Naturally and Artificially Flavored

12 FL OZ (354 mL)

MEIJER PHARMACIST RECOMMENED

MONEY BACK GURANTEE

DIST. BY MEIJER DISTRIBUTION, INC.

GRAND RAPIDS, MI 49544

www.meijer.com*This product is not manufactured or distributed by The Procter & Gamble Company, owner of the registered trademark ZzzQuil®.

meijer nighttime sleep-aid diphenhydramine HCl 50 mgmeijer nighttime sleep-aid diphenhydramine HCl 50 mg

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130708820059979GTIN-13: 0708820059979
EAN-13: 0708820059979
GTIN-12: 708820059979
UPC-A: 708820059979
GTIN storage (14 digits): 00708820059979		diphenydramine-fig1.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0e2e0f88-b076-afe1-4bdd-32bca4375becProduct name320250127
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
3e48c9c4-918d-5d23-2f0b-d2398b06be54Product name120140508
865c72dd-0d94-daac-f728-ddd4ded2a79eProduct name120140508

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
41250-73841250-738-12

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIPHENHYDRAMINE HYDROCHLORIDETC2D6JAD40ACTIB
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
FD&C RED NO. 40WZB9127XOAIACT
GLYCERINPDC6A3C0OXIACT
POTASSIUM CITRATEEE90ONI6FFIACT
WATER059QF0KO0RIACT
SODIUM BENZOATEOJ245FE5EUIACT
SORBITOL506T60A25RIACT
SUCRALOSE96K6UQ3ZD4IACT
XANTHAN GUMTTV12P4NEEIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
82025-10-24full-release2026-06-01 01:40:34
72024-10-18full-release2026-06-01 00:27:32

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
41f34160-4e1a-0167-e063-6394a90a9aaec7258241-2966-4876-918b-84bbf50ec4bc2025-10-24WarningsExact identifier
spl set id: c7258241-2966-4876-918b-84bbf50ec4bc

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.