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OTC products · Product label record

Sleep Aid drug information

DIPHENHYDRAMINE HCL
TARGET Corporation · ORAL

Product NDC: 11673-360

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameDIPHENHYDRAMINE HCL
Labeler / manufacturerTARGET Corporation
RouteORAL
Drug classDrug class not supplied in source label
Product NDC11673-360
Label effective date2026-09-02

Official product label reference

Sleep Aid — TARGET Corporation

This page contains 15 source sections for DIPHENHYDRAMINE HCL, oral route. Label set edfe32b5-9213-4350-9508-2530ee26c5d5, version 6.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

Use for relief of occasional sleeplessness.

Purpose

Purpose Nighttime sleep-aid
Dosage and administration — label text
Directions adults and children 12 years of age and over: 1 softgel (50 mg) at bedtime if needed, or as directed by a doctor
Warnings
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 trouble urinating due to an enlarged prostate gland Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers. When using this product avoid alcoholic drinks. 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 (1-800-222-1222) right away.
Active ingredient
Active ingredient (in each softgel) Diphenhydramine HCl 50 mg
Do not use
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
Ask a doctor before use if you have a breathing problem such as emphysema or chronic bronchitis glaucoma trouble urinating due to an enlarged prostate gland
Ask a doctor or pharmacist
Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers.
While using this medicine
When using this product avoid alcoholic drinks.
When to stop use and seek help
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.
Pregnancy or breast feeding
If pregnant or breast-feeding, ask a health professional before use.
Child safety
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
Storage and handling
Other information store between 15-30°C (59°-86°F)
Inactive ingredient
Inactive ingredients FD&C blue #1, gelatin, glycerin, lecithin, light mineral oil, mannitol, polyethylene glycol, purified water, sorbitol, sorbitan, white ink
Questions
Questions or comments? Call 1- 800-910-6874

Official sources and product identifiers

Substances listed: DIPHENHYDRAMINE HYDROCHLORIDE

RxNorm identifiers: 1020477

Package NDC codes

11673-360-32, 11673-360-60

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.