Diphenhydramine HCl description, usages, side effects, indications, overdosage, supplying and lots more!

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Diphenhydramine HCl

A&Z Pharmaceutical, Inc.
A&Z Pharmaceutical, Inc.

Diphenhydramine HCl Caplet 25mg Film Coated


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

USES

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: ■ sneezing ■ runny nose ■ itchy, watery eyes ■ itching of the nose or throat ■ and these symptoms associated with the common cold ■ sneezing ■ runny nose

WARNINGS

Do Not Use

with any other products containing diphenhydramine, including one applied topically

Ask a Doctor

before use if you have ■ a breathing problem such as emphysema or chronic bronchitis, ■ glaucoma or ■ trouble urinating due to an enlarged prostate gland

Ask a Doctor/Pharmacist before use

are taking sedatives or tranquilizers

When using this product

■ marked drowsiness may occur ■ avoid alcoholic beverages ■ alcohol, sedatives, and tranquilizers may increase drowsiness ■ be careful when driving a motor vehicle or operating machinery ■ excitability may occur, especially in children

If pregnant or breast-feeding,

ask a health professional before use

Keep Out of Reach of Children.

In case of accidental overdose, contact a doctor or Poison Control Center immediately.

■ take every 4 to 6 hours ■ do not take more than 6 doses in 24 hours

Adults and children 12 years of age and older 25 mg to 50 mg (1 to 2 caplets)
Children 6 to under 12 years of age 12.5 mg** to 25 mg (1 caplet)
Children under 6 years of age Consult a doctor

** A 12.5 mg dosage strength is not available in this package. (Do not attempt to break caplet)

■ store at room temperature in a dry place ■ do not use if blister package is torn

croscarmellose sodium, D&C Red #27, hydroxypropylmethyl cellulose, lactose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, silicon dioxide, titanium dioxide

DISPLAY PANEL

Diphenhydramine HCl

Diphenhydramine HCl TABLET, COATED

Product Information

Product Type Human otc drug label Item Code (Source) NDC:62211-048(NDC:048)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DIPHENHYDRAMINE HYDROCHLORIDE DIPHENHYDRAMINE 25 mg

Inactive Ingredients

Ingredient Name Strength
CROSCARMELLOSE SODIUM
D&C RED NO. 27
MAGNESIUM STEARATE
hypromellose

Product Characteristics

Color Size Imprint Code Shape
pink 12 mm AZ048 CAPSULE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:62211-048-93 24 in 1 BLISTER PACK
2 NDC:62211-048-01 100 in 1 BOTTLE
3 NDC:62211-048-99 69767 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part343 2003-03-10


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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