JET-ASLEEP DOUBLE STRENGTH NIGHT TIME SLEEP AID- diphenhydramine hydrochloride tablet

Jet-Asleep Double Strength Night Time Sleep Aid by

Drug Labeling and Warnings

Jet-Asleep Double Strength Night Time Sleep Aid by is a Otc medication manufactured, distributed, or labeled by Bell Pharmaceuticals, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient (in each caplet)

Diphenhydramine HCL 50mg

Purpose

Nighttime sleep-aid

Uses

• for relief of occasional sleeplessness

Warnings

Do not use

• in 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
• traouble urinating due to a to enlarged prostate gland
• glaucome 

Ask a doctor or pharmacist before useif you are 

• taking Sedatives or tranquilizers

When using this product

avoid alcoholic drinks

Stop use and ask a doctor

if sleeplessness lasts continuosly 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.

Keep out of reach of children.

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

Directions

• adults and children 12 years and over: take 1 caplets at bedtime if needed, or as directed by a doctor
• children under 12 years: do not ues

Other information

• each caplet contains:calcium 35 mg
• store between 15°-30°C (59°-86°F)
• don not use if tamper-evident seal is broken or missing

Inactive ingredients

colloidal silicon dioxide, croscarmellose sodium, dibasic calcium phosphate dihydrate, FD & C blue #1 aluminum lake, hypromellose, magnesium stearate, microcrystalline cellulose, mineral oil, stearic acid

Questions or comments?

1-800-328-5890 Weekdays 8:30-5:00 CST

Package Labeling:

INGREDIENTS AND APPEARANCE

JET-ASLEEP DOUBLE STRENGTH NIGHT TIME SLEEP AID 
diphenhydramine hydrochloride tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 15579-828
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

Inactive Ingredients
Ingredient Name	Strength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
MINERAL OIL (UNII: T5L8T28FGP)
STEARIC ACID (UNII: 4ELV7Z65AP)

Product Characteristics
Color	blue	Score	no score
Shape	OVAL	Size	14mm
Flavor		Imprint Code	350
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 15579-828-23	3 in 1 BOX	10/07/2017
1		8 in 1 BLISTER PACK; Type 0: Not a Combination Product
2	NDC: 15579-828-17	1 in 1 BOX	10/07/2017
2		100 in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part338	10/07/2017

Labeler - Bell Pharmaceuticals, Inc. (140653770)