BONINE- meclizine hydrochloride tablet, chewable

Bonine by

Drug Labeling and Warnings

Bonine by is a Otc medication manufactured, distributed, or labeled by Insight Pharmaceuticals. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

Active ingredient (in each tablet)

Meclizine HCl 25 mg

Purpose

Antiemetic

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

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

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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

INGREDIENTS AND APPEARANCE

BONINE 
meclizine hydrochloride tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63736-124
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
meclizine hydrochloride (UNII: HDP7W44CIO) (meclizine - UNII:3L5TQ84570)	meclizine	25 mg

Inactive Ingredients
Ingredient Name	Strength
crospovidone (UNII: 68401960MK)
FD&C Red No. 40 (UNII: WZB9127XOA)
Aluminum Oxide (UNII: LMI26O6933)
Lactose (UNII: J2B2A4N98G)
Magnesium Stearate (UNII: 70097M6I30)
Silicon Dioxide (UNII: ETJ7Z6XBU4)
Saccharin Sodium (UNII: SB8ZUX40TY)
stearic acid (UNII: 4ELV7Z65AP)
Croscarmellose Sodium (UNII: M28OL1HH48)

Product Characteristics
Color	PINK (light pink)	Score	2 pieces
Shape	ROUND	Size	9mm
Flavor	RASPBERRY, VANILLA	Imprint Code	Bonine;201
Contains

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
OTC monograph final	part336	06/08/2009

Labeler - Insight Pharmaceuticals (176792315)