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

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Diphenhydramine

Rebel Distributors Corp

Diphenhydramine Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Diphenhydramine HCl 25mg

Diphenhydramine HCl 50mg

Purpose

Antihistamine

Keep Out of Reach of Children

Diphenhydramine Uses

Temporarily relieves: ° hay fever or other upper respiratory allergies like: ° runny nose

° sneezing ° watery eyes ° itchy nose or throat

Warnings

Do not use with any other product containing Diphenhydramine HCl, including one applied topically.

Ask a doctor or pharmacist before use if you have ° trouble urinating due to enlarged prostate gland ° a breathing problem such as emphysema or chronic bronchitis ° glaucoma ° if you are taking sedatives or tranquilizers

When using this product ° avoid alcoholic drinks ° marked drowsiness may occur ° excitability may occur, especially in children ° alcohol, sedatives & tranquilizers may increase drowsiness ° be careful when driving a motor vehicle or operating machinery.

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

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

Directions

° take every 4-6 hours

° do not take more than 6 doses in 24 hours.

Adults & children 12 years & over: 1-2 capsules

Children 6 to under 12 years: 1 capsule

Children under 6: ask a doctor

Other Information

Store at room temperature 15°-30°C (59°-86°F)

Protect from excessive moisture

Inactive ingredients

Lactose Monohydrate, Silicon Dioxide, Magnesium Steareate, Black Iron Oxide, Gelatin, Sodium Lauyl Sulfate, D&C Red No. 28, FD&C Red No. 40, FD&C Blue No. 1.

Distributed by:

SDA Laboratories, Inc.

Greenwich, CT 06830

Repackaged by:

Rebel Distributors Corp

Thousand Oaks, CA 91320

Package/Label Principal Display Panel

Diphenhydramine

Package/Label Principal Display Panel

Diphenhydramine

Diphenhydramine

Diphenhydramine CAPSULE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:21695-304(NDC:66424-020)
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
lactose monohydrate
SILICON DIOXIDE
MAGNESIUM STEARATE
FERROSOFERRIC OXIDE
GELATIN
SODIUM LAURYL SULFATE
D&C RED NO. 28
FD&C RED NO. 40
FD&C BLUE NO. 1

Product Characteristics

Color Size Imprint Code Shape
PINK (Pink/White) 15 mm PH;014 CAPSULE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:21695-304-15 15 in 1 BOTTLE
2 NDC:21695-304-20 20 in 1 BOTTLE
3 NDC:21695-304-24 24 in 1 BOTTLE
4 NDC:21695-304-30 30 in 1 BOTTLE
5 NDC:21695-304-90 90 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2007-01-01


Diphenhydramine

Diphenhydramine CAPSULE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:21695-500(NDC:66424-021)
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
lactose monohydrate
SILICON DIOXIDE
MAGNESIUM STEARATE
FERROSOFERRIC OXIDE
GELATIN
SODIUM LAURYL SULFATE
D&C RED NO. 28
FD&C RED NO. 40
FD&C BLUE NO. 1

Product Characteristics

Color Size Imprint Code Shape
PINK 15 mm PH;013 CAPSULE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:21695-500-15 15 in 1 BOTTLE
2 NDC:21695-500-20 20 in 1 BOTTLE
3 NDC:21695-500-30 30 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2007-01-01


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