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Bonine

Insight Pharmaceuticals

BONINE MECLIZINE HYDROCHLORIDE • ANTIEMETIC


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient (in each tablet)

Meclizine HCl 25 mg

Purpose

Antiemetic

Bonine Uses

prevents and treats nausea, vomiting or dizziness associated with motion sickness

Warnings

Do not use for children under 12 years of age unless directed by a doctor

Do not take unless directed by a doctor if you have

  • glaucoma
  • trouble urinating due to an enlarged prostate gland
  • a breathing problem such as emphysema or chronic bronchitis

Do not take if you are taking sedatives or tranquilizers, without first consulting your doctor.

When using this product

  • do not exceed recommended dosage
  • 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.

Directions

  • dosage should be taken one hour before travel starts
  • adults and children 12 years of age and over: take 1 to 2 tablets once daily or as directed by a doctor

Bonine Other information

store at room temperature 20°– 25°C (68°–77°F)

Inactive ingredients

Croscarmellose Sodium, Crospovidone, FD&C Red #40 Lake, Lactose, Magnesium Stearate, Raspberry Flavor, Silica, Sodium Saccharin, Stearic Acid, Vanilla Flavor.

Questions?

call 1-800-344-7239 or visit us on the web at www.insightpharma.com

Dist. by: INSIGHT Pharmaceuticals Corp.
Langhorne, PA 19047-1749

PRINCIPAL DISPLAY PANEL - 8 Tablet Carton

BONINE ®
MECLIZINE HYDROCHLORIDE • ANTIEMETIC

Prevents Motion Sickness

Chewable
Once-A-Day
Protection

8 Tablets

Bonine

Bonine

meclizine hydrochloride TABLET, CHEWABLE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:63736-124
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MECLIZINE HYDROCHLORIDE MECLIZINE 25 mg

Inactive Ingredients

Ingredient Name Strength
CROSPOVIDONE
FD&C RED NO. 40
ALUMINUM OXIDE
LACTOSE
MAGNESIUM STEARATE
SILICON DIOXIDE
saccharin sodium
STEARIC ACID
CROSCARMELLOSE SODIUM

Product Characteristics

Color Size Imprint Code Shape
PINK (light pink) 9 mm Bonine;201 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:63736-124-08 8 in 1 BOX
2 NDC:63736-124-12 12 in 1 BOX
3 NDC:63736-124-16 16 in 1 BOX
4 NDC:63736-124-21 21 in 1 BOX
5 NDC:63736-124-95 2 in 1 POUCH

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part336 2009-06-08


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Be sure to consult your doctor before taking any medication!
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