NIGHT TIME SLEEP-AID- diphenhydramine hcl liquid

NIGHT TIME SLEEP-AID by

Drug Labeling and Warnings

NIGHT TIME SLEEP-AID by is a Otc medication manufactured, distributed, or labeled by Discount Drug Mart. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug FactsActive ingredients (in each 30 mL dose cup or 2 tablespoons)

Diphenhydramine HCL 50 mg

Purpose

Nighttime sleep-aid

Kep out of reach of children

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

Uses

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

Warnings

DO NOT USE IF IMPRINTED SHRINK BAND IS MISSING OR BROKEN

Failure to follow these warnings could result in serious consequences.

Do not use

• for children under 12 years of age.
• with any other product containing diphenhydramine, even one used on skin
• with any other drugs that cause drowsiness such as antihistamines and nighttime cough, cold/flu products

Ask a doctor before use if you have

• heart disease
• trouble urinating due to an enlarged prostate gland
• glaucoma
• a breathing problem such as asthma, emphysema or chronic bronchitis

Ask a doctor or pharmacist before use if you are

taking sedatives or tranquilizers or any other sleep aid

When using this product

• do not use more than directed
• avoid alcoholic beverages and other drugs that cause drowsiness
• drowsiness will occur
• be careful driving a motor vehicle or operating machinery
• alcohol, sedatives, and tranquilizers may increase drowsiness

Stop use and ask a doctor if

sleeplessness persists continously for more than 2 weeks. Insomnia may be a symptom of serious underlying medical illness.

If pregnant or breast feeding,

ask a health professional before use.

Directions

• take only as recommended
• use dosage cup or tablespoon

• Age: Dose
• Adults and children 12 years and over: One dose = 2 tablespoons (30 mL) at bedtime if needed or as directed by a doctor
• Children under 12 years: Do not use

Other information

• each 30 mL dose (2 tablespoons) contains: sodium 23 mg
• dosage cup provided
• store at room temperature

Inactive ingredients

citric acid, FD and C Blue # 1, FD and C Red # 40, flavor, high fructose corn syrup, poloxamer 407, propllene glycol, purified water, sodium benzoate, sodium citrate, sodium saccharin

Questions?

Call weekdays from 9:30 AM to 4:30 PM EST at 1-877-798-5944

DISCOUNT drug mart FOOD FAIR NIGHT TIME SLEEP-AID product label

* COMPARE TO THE ACTIVE INGREDIENT IN ZzzQuil™NIGHTTIME SLEEP-AID

DISCOUNT

drug mart

FOOD FAIR

NIGHT TIME SLEEP-AID

Diphenhydramine HCL

Non-Habit Forming

Warming Berry Flavored Liquid

Not for treating Cold or Flu

12 FL OZ (354 mL)

* This product is not manufactured or distributed by Proctor and Gamble owner of the registered trademark ZzzQuil™

LR-055

SATISFACTION GUARANTEED

IF DISSATISFIED, RETURN UNUSED PORTION AND PACKAGE TO THE STORE WHERE PURCHASED. IF UNABLE TO RETURN TO THE STORE, SEND REASON FOR DISSATISFACTION , NAME, ADDRESS AND EMPTY PACKAGE TO: DISCOUNT DRUG MART, 211 COMMERCE DRIVE MEDINNA, OHIO 44256

INGREDIENTS AND APPEARANCE

NIGHT TIME SLEEP-AID 
diphenhydramine hcl liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53943-522
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M)	DIPHENHYDRAMINE HYDROCHLORIDE	50 mg  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C RED NO. 40 (UNII: WZB9127XOA)
HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)
POLOXAMER 407 (UNII: TUF2IVW3M2)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)

Product Characteristics
Color		Score
Shape		Size
Flavor	BERRY (BERRY)	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53943-522-25	117 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/10/2013
2	NDC: 53943-522-28	354 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/10/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part338	12/10/2013

Labeler - Discount Drug Mart (047741335)