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

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diphenhydramine hydrochloride

Eon Labs, Inc.

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient (in each capsule)

Diphenhydramine Hydrochloride 25 mg

Diphenhydramine Hydrochloride 50 mg

Purpose

Antihistamine

diphenhydramine hydrochloride Uses

Temporarily relieves these symptoms due to hay fever or other upper respiratory allergies

  • runny nose and sneezing
  • itching of the nose or throat
  • itchy, watery eyes.

Warnings

Ask a doctor before use if you have

  • a breathing problem such as emphysema or chronic bronchitis
  • glaucoma
  • difficulty in urination due to enlargement of the prostate gland

Do not use with ny other product containing diphenhydramine, including products used topically.

Ask a doctor or pharmacist before use if you are

  • taking tranquilizers or sedatives
  • taking other products containing diphenhydramine

When using this product

  • Do not exceed recommended dosage
  • excitability may occur, especially in children
  • marked drowsiness may occur
  • alcohol, sedatives, and tranquilizers may increase drowsiness
  • avoid alcoholic drinks
  • use caution when driving a motor vehicle or operating machinery

If pregnant or breastfeeding ask a health professional before use.

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

Directions

  • Adults and Children 12 years and over: 25 to 50 mg (1 to 2 capsules) every 4 to 6 hours, not to exceed 12 capsules in 24 hours.
  • Children 12 years and under: Consult a Doctor

Inactive ingredients

Colloidal Silicon Dioxide, Corn Starch, D&C Red #28, FD&C Blue #1, FD&C Red #40, Gelatin, Anhydrous Lactose, Magnesium Stearate, Silicon Dioxide and Sodium Lauryl Sulfate.

Storage and Handling

Keep tightly closed. Store at 20º to 25ºC (68º to 77ºF) [See USP Controlled Room Temperature].

Manufactured for Sandoz Inc.

Princeton, NJ 08540

Manufactured by Epic Pharma, LLC

Laurelton, NY 11413

L1812

Rev. 11/08

Package Label - Principal Display Panel

NDC 0185-0648-30

DiphenhydrAMINE

Hydrochloride

Capsules USP

25 mg

30 Capsules

Manufactured for Sandoz Inc.

Princeton, NJ 08540

Manufactured by Epic Pharma, LLC

Laurelton, NY 11413

Sandoz

diphenhydramine hydrochloride

 

Package Label - Principal Display Panel

NDC 0185-0649-30

DiphenhydrAMINE

Hydrochloride

Capsules USP

50 mg

30 Capsules

Manufactured for Sandoz Inc.

Princeton, NJ 08540

Manufactured by Epic Pharma, LLC

Laurelton, NY 11413

Sandoz

diphenhydramine hydrochloride

diphenhydramine hydrochloride

diphenhydramine hydrochloride CAPSULE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0185-0648
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
SILICON DIOXIDE
STARCH, CORN
D&C RED NO. 28
FD&C BLUE NO. 1
FD&C RED NO. 40
GELATIN
ANHYDROUS LACTOSE
MAGNESIUM STEARATE
SILICON DIOXIDE
SODIUM LAURYL SULFATE

Product Characteristics

Color Size Imprint Code Shape
PINK (pink top/clear body) 14 mm E648 CAPSULE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0185-0648-30 30 in 1 BOTTLE
2 NDC:0185-0648-53 50 in 1 BOTTLE
3 NDC:0185-0648-01 100 in 1 BOTTLE
4 NDC:0185-0648-10 1000 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2000-05-01


diphenhydramine hydrochloride

diphenhydramine hydrochloride CAPSULE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0185-0649
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DIPHENHYDRAMINE HYDROCHLORIDE DIPHENHYDRAMINE 50 mg

Inactive Ingredients

Ingredient Name Strength
SILICON DIOXIDE
STARCH, CORN
D&C RED NO. 28
FD&C BLUE NO. 1
FD&C RED NO. 40
GELATIN
ANHYDROUS LACTOSE
MAGNESIUM STEARATE
SILICON DIOXIDE
SODIUM LAURYL SULFATE

Product Characteristics

Color Size Imprint Code Shape
PINK (pink top/pink body) 14 mm E649 CAPSULE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0185-0649-30 30 in 1 BOTTLE
2 NDC:0185-0649-53 50 in 1 BOTTLE
3 NDC:0185-0649-01 100 in 1 BOTTLE
4 NDC:0185-0649-10 1000 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2000-05-01


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