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

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Dimenhydrinate

Qualitest Pharmaceuticals

DIMENHYDRINATE TABLETS, USP 50 mg


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Dimenhydrinate 50 mg

Antiemetic

Uses

Uses for prevention and treatment of these symptoms associated with motion sickness:

  • nausea
  • vomiting
  • dizziness

Do not use in children under 2 years of age unless directed by a doctor

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

Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers

When using this product

  • marked drowsiness may occur
  • alcohol, sedatives and tranquilizers may increase drowsiness
  • avoid alcoholic drinks
  • be careful when driving a motor vehicle or operating machinery

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. (1-800-222-1222).

  • to prevent motion sickness, the first dose should be taken 1/2 to 1 hour before starting activity
  • to prevent or treat motion sickness, use the following dosing

adults and children
12 years and over 

1-2 tablets every 4-6 hours; not more than
8 tablets in 24 hours, or as directed by a doctor 

children 6 years to
under 12 years 

1/2-1 tablet every 6-8 hours; not more than
3 tablets in 24 hours, or as directed by a doctor 

children 2 years to
under 6 years 

1/4-1/2 tablet every 6-8 hours; not more than
1 1/2 tablets in 24 hours, or as directed by a doctor 

store at 15° to 30°C (59° to 86°F)

You may report serious side effects to: 130 Vintage Drive, Huntsville, AL 35811.

colloidal silicone dioxide, lactose monohydrate, magnesium stearate, microcrystalline cellulose, sodium starch glycolate, stearic acid

Made in the USA
for Qualitest Pharmaceuticals
Huntsville, AL 35811

Rev. 8/09 R4
8080234 0111

PRINCIPAL DISPLAY PANEL

Dimenhydrinate

 

Dimenhydrinate

Dimenhydrinate TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0603-3327
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DIMENHYDRINATE DIPHENHYDRAMINE 50 mg

Inactive Ingredients

Ingredient Name Strength
SILICON DIOXIDE
lactose monohydrate
MAGNESIUM STEARATE
cellulose, microcrystalline
SODIUM STARCH GLYCOLATE TYPE A POTATO
STEARIC ACID

Product Characteristics

Color Size Imprint Code Shape
WHITE 9 mm 0111;V ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0603-3327-21 100 in 1 BOTTLE, PLASTIC
2 NDC:0603-3327-32 1000 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part336 2004-03-01


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Be sure to consult your doctor before taking any medication!
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