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Nighttime Sleep Aid

Dosage form
CAPSULE, LIQUID FILLED
Labeler
PuraCap Pharmaceutical LLC
Label updated
2019-12-11
Retrieved
2026-09-07
Active ingredients
DIPHENHYDRAMINE HYDROCHLORIDE
View original label and images on DailyMed ↗
Label information

Drug Facts

Active ingredient (in each softgel)

Diphenhydramine HCl 50 mg

Purpose

Nighttime sleep-aid

Use
  • for relief of occasional sleeplessness
주의사항

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

Label information

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

Label information

When using this product avoid alcoholic drinks

Label information

Stop use and ask a doctor if sleeplessness persist continuously for more than 2 weeks. Insomnia may be a symptom of serious underlying medical illness.

Label information

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

Label information

Keep out of reach of children. 

Label information

In case of overdose, get medical help or contact a Poison Control Center right away.

Directions
  • adults and children 12 years of age and over: 1 softgel (50 mg) at bedtime if needed, or as directed by a doctor
Other Information
  • Store at 15°-30°C (59°-86°F)
  • Keep outer carton for complete warnings and product information 
Inactive ingredients

FD&C blue #1, gelatin, glycerin, polyethylene glycol, purified water, sorbitol special and white edible ink

Questions or comments?

Call toll free: 1-800-833-6278

PRINCIPAL DISPLAY PANEL

Nighttime Sleep Aid 32ct Diphenhydramine HCl 50mg compare to the active ingredient in Unisom® Sleep Gels® NDC 51013-142-16

[Image in the official label — see DailyMed source]

[Image in the official label — see DailyMed source]

DailyMed Set ID: 5d9658b0-99df-4851-a082-84e2e7ddc2c4 · Version 2
NDC: 51013-142