BONINE- meclizine hydrochloride tablet, chewable

BONINE by

Drug Labeling and Warnings

BONINE by is a Otc medication manufactured, distributed, or labeled by WellSpring Pharmaceutical Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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 

in children under 12 years of age unless directed by a doctor.

Ask a doctor before use if you have

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

Ask a doctor or pharmacist before use if you are

taking sedatives or tranquilizers.

When using this product

• avoid alcoholic beverages
• alcohol, sedatives, and tranquilizers may increase drowsiness
• drowsiness may occur
• use caution 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
• chew or crush tablets completely before swallowing; do not swallow tablets whole
• adults and children 12 years and over: take 1 to 2 chewable tablets once daily or as directed by a doctor

Other information

• store at 25˚C (77˚F); excursions permitted between 15˚-30˚C (59˚-86˚F)
• see end flap for expiration date and lot number
• protect from heat and humidity

Inactive ingredients

colloidal silicon dioxide, dextrose, FD&C red #40 aluminum lake, flavor, lactose monohydrate, magnesium stearate, pregelatinized starch, propylene glycol, saccharin sodium, silicon dioxide

Questions or comments?

1 (844) 241-5454 or www.bonine.com 

Dist. by:

WellSpring Pharmaceutical
Corporation Sarasota, FL 34243
©2024 WellSpring Pharmaceutical Corporation

TAMPER EVIDENT: DO NOT USE IF PRINTED TEAR STRIP IS BROKEN OR MISSING

MONEY BACK GUARANTEE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL 65197-297

*Less drowsy vs. Dramamine® dimenhydrinate. Dramamine® is a registered trademark of Medtech Products Inc.

NEW LOOK! Same great formula

9X the Adventure** Meclizine HCl Antiemetic 25 mg

Bonine 12 ct

INGREDIENTS AND APPEARANCE

BONINE 
meclizine hydrochloride tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65197-297
Route of Administration	ORAL

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

Inactive Ingredients
Ingredient Name	Strength
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
FD&C RED NO. 40 (UNII: WZB9127XOA)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
STARCH, CORN (UNII: O8232NY3SJ)
MAGNESIUM STEARATE (UNII: 70097M6I30)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)

Product Characteristics
Color	pink	Score	2 pieces
Shape	ROUND	Size	9mm
Flavor	RASPBERRY	Imprint Code	BONINE
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65197-297-08	1 in 1 BOX	04/01/2025
1		8 in 1 BLISTER PACK; Type 0: Not a Combination Product
2	NDC: 65197-297-12	1 in 1 BOX	04/01/2025
2		12 in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC: 65197-297-16	2 in 1 BOX	04/01/2025
3		8 in 1 BLISTER PACK; Type 0: Not a Combination Product
4	NDC: 65197-297-24	3 in 1 CARTON	04/01/2025
4		8 in 1 BLISTER PACK; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M009	04/01/2025

Labeler - WellSpring Pharmaceutical Corporation (110999054)