BONINE MAX

Manufacturer: WellSpring Pharmaceutical Corporation
Effective date: 2025-04-11
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-06-01 00:59:02

Label at a glance#

ProductBONINE MAX

Active ingredientMECLIZINE HYDROCHLORIDE

Label structure10 sections

Indications and uses

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

Dosage and administration

• do not take more than directed • dosage should be taken one hour before travel starts • Chew or crush tablet completely before swallowing; do not swallow tablet whole • adults and children 12 years of age and over: take 1 chewable tablet once daily or as directed by a doctor.

Storage and handling

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

Contacts and useful links#

PhoneLabel contact1 (844) 241-5454

Websitewww.bonine.com

www.bonine.com

Label contents#

Full prescribing information#

Active ingredient (in each tablet)

OTC - ACTIVE INGREDIENT SECTION

Meclizine HCl 50 mg

Purpose

OTC - PURPOSE SECTION

Antiemetic

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

Do not use

OTC - DO NOT USE SECTION

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

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

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

SPL UNCLASSIFIED SECTION

taking sedatives or tranquilizers.

When using this product

OTC - WHEN USING SECTION

alcohol, sedatives, and tranquilizers may increase drowsiness
use caution when driving a motor vehicle or operating machinery
drowsiness may occur
avoid alcoholic drinks

If pregnant or breast-feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

• do not take more than directed

• dosage should be taken one hour before travel starts

• Chew or crush tablet completely before swallowing; do not swallow tablet whole

• adults and children 12 years of age and over: take 1 chewable tablet once daily or as directed by a doctor.

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

corn starch, FD&C red #40 aluminum lake, flavor, lactose anhydrous, magnesium stearate, sodium saccharin, silicon dioxide

Questions?

OTC - QUESTIONS SECTION

call toll-free 1 (844) 241-5454 or visit us on the web at www.bonine.com

SPL UNCLASSIFIED SECTION

NDC 65197-520-16

BONINE MAX STRENGTH

Prevents and treats: Dizziness - Nausea - Vomiting - Motion sickness

** Results may vary

ATTENTION: DO NOT USE IF CARTON IS OPEN OR IF BLISTER IS TORN OR MISSING. Keep carton for important drug facts information.

MONEY BACK GUARANTEED

Dist. by: WellSpring Pharmaceutical Corporation
Sarasota, FL 34243 USA

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NEW!

9x the Adventure**

Meclizine HCL - Antiemetic 50 mg

Prevents and treats: Dizziness - Nausea - Vomiting - Motion sickness

50 mg MECLIZINE HCL

Nothing Stronger without a PrescriptionBonine MAX

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2632643	meclizine HCl 50 MG Chewable Tablet	PSN	4
2632643	meclizine hydrochloride 50 MG Chewable Tablet	SCD	4

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
MECLIZINE Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
ac6963c4-31c6-325f-ee58-83a0a06597ad	Product name	5	20221206

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
65197-520-16	BONINE MAX	2 in 1 BOX	TABLET, CHEWABLE	2	4
65197-520-16	BONINE MAX	8 in 1 BLISTER PACK	TABLET, CHEWABLE	8	4
65197-520-17	BONINE MAX	2 in 1 BOX	TABLET, CHEWABLE	2	4
65197-520-17	BONINE MAX	8 in 1 BLISTER PACK	TABLET, CHEWABLE	8	4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
65197-520	BONINE MAX (MECLIZINE HYDROCHLORIDE) TABLET, CHEWABLE [WELLSPRING PHARMACEUTICAL CORPORATION]	4	Current NDC, 4 package rows	20250413_7326a47e-284e-4b6f-8eb0-7933dc1e3f0d.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

BONINE MAX
meclizine hydrochloride
MECLIZINE
ANHYDROUS LACTOSE
STARCH, CORN
PEPPERMINT
FD&C RED NO. 40
SACCHARIN SODIUM
MAGNESIUM STEARATE
SILICON DIOXIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
65197-520	65197-520-17, 65197-520-16

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MECLIZINE HYDROCHLORIDE	HDP7W44CIO	ACTIB
ANHYDROUS LACTOSE	3SY5LH9PMK	IACT
STARCH, CORN	O8232NY3SJ	IACT
PEPPERMINT	V95R5KMY2B	IACT
FD&C RED NO. 40	WZB9127XOA	IACT
SACCHARIN SODIUM	SB8ZUX40TY	IACT
MAGNESIUM STEARATE	70097M6I30	IACT
SILICON DIOXIDE	ETJ7Z6XBU4	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
BONINE MAX	MECLIZINE HYDROCHLORIDE	WellSpring Pharmaceutical Corporation	7326a47e-284e-4b6f-8eb0-7933dc1e3f0d	2025-04-11	Warnings	Exact identifier ndc (package): 65197-520-17 ndc (package): 65197-520-16 ndc (product): 65197-520 ndc11 (package): 65197052017 ndc11 (package): 65197052016 spl id: 610a37d5-4aa5-49cf-b50c-0ddda9d1d026 spl set id: 7326a47e-284e-4b6f-8eb0-7933dc1e3f0d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.