Rite Aid Nighttime Sleep Aid

Manufacturer
RITE AID CORPORATION
Effective date
2024-10-30
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:32:13

Label at a glance#

ProductRite Aid Nighttime Sleep Aid Non Habit Forming
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 provided   adults & children 12 yrs & over   30 mL at bed time if needed or as directed by a doctor   children under 12 yrs   do not use

Storage and handling

• each 30 mL dose contains: sodium 10 mg • store at room temperature

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient (in each 30 mL dose cup)

OTC - ACTIVE INGREDIENT SECTION

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

OTC - DO NOT USE SECTION

  • 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

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers

When using this product

OTC - WHEN USING SECTION

  • avoid alcoholic beverages

OTC - STOP USE SECTION

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.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

SPL UNCLASSIFIED SECTION

In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

Directions

DOSAGE & ADMINISTRATION SECTION

  • take only one dose per day (24 hours)
  • measure with dosing cup provided
  1. adults & children 12 yrs & over
  1. 30 mL at bed time if needed or as directed by a doctor
  1. children under 12 yrs
  1. do not use

Other information

STORAGE AND HANDLING SECTION

  • each 30 mL dose contains: sodium 10 mg
  • store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

anhydrous citric acid, flavor, glycerin, potassium citrate, purified water, sodium benzoate, sorbitol, sucralose, xanthan gum.

Questions or comments?

OTC - QUESTIONS SECTION

1-866-467-2748

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Compare to the active ingredient in ZzzQuil™ Nighttime Sleep-Aid*

NDC# 11822-7530-1

Nighttime

Sleep-aid

Diphenhydramine HCl

Non-Habit Forming

Makes you fall asleep fast

Sugar-Free,

  • Dye-Free,
  • Aspartame-Free

Berry Flavor

Naturally and Artificially Flavored

No added alcohol

Not for Pain. Not for Colds. Just for Sleep

12 FL. OZ. (354 mL)

*This product is not manufactured or distributed by Procter & Gamble, the distributor of ZzzQuil™Nighttime Sleep-Aid.

Distributed by

Rite Aid Nighttime Sleep Aid Diphenhydramine HCL
Rite Aid Nighttime Sleep Aid Diphenhydramine HCL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1248354diphenhydrAMINE HCl 50 MG in 30 mL Oral SolutionPSN5
1248354diphenhydramine hydrochloride 1.67 MG/ML Oral SolutionSCD5
1248354diphenhydramine HCl 1.667 MG/ML Oral SolutionSY5
1248354diphenhydramine HCl 50 MG per 30 ML Oral SolutionSY5

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
DIPHENHYDRAMINE Pharmacologic Class Indexing3Indexing - Pharmacologic Class20180813

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11822-7530-1Rite Aid Nighttime Sleep AidNon Habit Forming354 mL in 1 BOTTLE, PLASTICLIQUID3545

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-7530RITE AID NIGHTTIME SLEEP AID NON HABIT FORMING (DIPHENHYDRAMINE HYDROCHLORIDE) LIQUID [RITE AID CORPORATION]5Current NDC, Legacy NDC, 1 package rows20241101_59ba6824-fa6c-4b3f-9f1f-ea194766c8a1.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11822-753011822-7530-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML

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
Rite Aid Nighttime Sleep Aid Non Habit FormingDIPHENHYDRAMINE HYDROCHLORIDERITE AID CORPORATION59ba6824-fa6c-4b3f-9f1f-ea194766c8a12024-10-30WarningsExact identifier
ndc (package): 11822-7530-1
ndc (product): 11822-7530
ndc11 (package): 11822753001
spl id: a62f70a1-3c7f-4069-b361-52bde8513b08
spl set id: 59ba6824-fa6c-4b3f-9f1f-ea194766c8a1

Reported adverse events (FAERS/openFDA)#

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