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Sleepeze

Dosage form
TABLET
Labeler
Medtech Products Inc.
Label updated
2024-01-18
Retrieved
2026-09-07
Active ingredients
DIPHENHYDRAMINE HYDROCHLORIDE
View original label and images on DailyMed ↗
Label information

Drug   Facts

Purpose

Diphenhydramine Hydrochloride 50 mg………………..Nighttime sleep aid

Uses

● relieves occasional sleeplessness ● helps to reduce difficulty falling asleep

Warnings

Do not use

●if you are elderly, as this drug may cause excitation rather than sedation ●with any other product containing diphenhydramine, even one used on skin ●in children under 12 years of age

Ask a doctor or pharmacist before use if you

●have ▪a breathing problem such as emphysema or chronic bronchitis ▪glaucoma ▪difficulty urinating ●take sedatives or tranquilizers ●are pregnant or breastfeeding

When using this product

avoid drinking alcohol.

Stop use and ask a doctor if

sleeplessness continues for more than 2 weeks. Sleeplessness may be a symptom of a serious underlying medical illness.

Keep out of reach of children.

In case of overdose, call a poison control centre or get medical help right away.

Directions

Adults and children 12 years and over: ▪ take 1 tablet at bedtime if needed, or as directed by a doctor ▪ if you feel drowsy in the morning, consult a doctor or pharmacist as you may require a lower dosage (25 mg) ▪ do not take more than directed

Other information

 Store at 20° to 25°C

Inactive ingredients

anhydrous dibasic calcium phosphate, croscarmellose sodium, FD&C blue no. 1 aluminum lake, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, mineral oil, silicon dioxide, stearic acid, talc, titanium dioxide, triacetin, water

SECURITY   FEATURE:   Safety   sealed   in   individual   pouches.   Do   not   use   if   pouch   is   not   safely   sealed.

Important:   Keep   carton   for   future   reference.

PRINCIPAL DISPLAY PANEL

Sleep.eze
Extra strength

Caplets

10 coated capsules

[Image in the official label — see DailyMed source]

DailyMed Set ID: 31d3dcb1-0898-4fee-b236-2f1096b0d787 · Version 2
NDC: 63029-921