Motion Sickness Relief

Manufacturer: PuraCap Pharmaceutical LLC | Advance Pharmaceutical Inc.
Effective date: 2017-11-28
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:53:07

Label at a glance#

ProductMotion Sickness Relief

Active ingredientMECLIZINE HYDROCHLORIDE

Label structure9 sections

Indications and uses

for prevention and treatment of these symptoms associated with motion sickness: nausea vomiting dizziness

Dosage and administration

take first dose one hour before starting activity adults and children 12 years and over: 1 to 2 tablets once daily, or as directed by a doctor

Storage and handling

Phenylketonurics: each tablet contains : phenylalanine 0.28 mg store at room temperature 15º - 30ºC (59º - 86ºF)

Contacts and useful links#

PhonePoison Help1-800-222-1222

PhoneLabel contact1-855-215-8180

Label contents#

Full prescribing information#

Active ingredient (in each tablet)

OTC - ACTIVE INGREDIENT SECTION

Meclizine Hydrochloride 25 mg

Purpose

OTC - PURPOSE SECTION

Antiemetic

Uses

INDICATIONS & USAGE SECTION

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

nausea
vomiting
dizziness

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

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

Ask a doctor or pharmacist before use if you are

OTC - ASK DOCTOR/PHARMACIST SECTION

taking sedatives or tranquilizers

When using this product

OTC - WHEN USING SECTION

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

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a doctor 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 (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

take first dose one hour before starting activity
adults and children 12 years and over: 1 to 2 tablets once daily, or as directed by a doctor

Other information

STORAGE AND HANDLING SECTION

Phenylketonurics: each tablet contains: phenylalanine 0.28 mg
store at room temperature 15º - 30ºC (59º - 86ºF)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aspartame, compressible sugar, croscarmellose sodium, dextrose, FD&C red 40 (al-lake), magnesium stearate, microcrystalline cellulose, raspberry flavor

Questions or comments?

OTC - QUESTIONS SECTION

Call toll free: 1-855-215-8180

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Motion Sickness Relief

30 Tablets 15 Pouches (2 Tablets per Pouch)

NDC 51013-322-54

CVSF36-00

CVSB36-00

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
995632	meclizine HCl 25 MG Chewable Tablet	PSN	1
995632	meclizine hydrochloride 25 MG Chewable Tablet	SCD	1

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
ed912195-5da0-0f2f-6f4b-3ef17710cbe3	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
51013-322-54	Motion Sickness Relief	15 in 1 CARTON	TABLET, CHEWABLE	15		1
51013-322-54	Motion Sickness Relief	2 in 1 POUCH	TABLET, CHEWABLE	2		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51013-322	MOTION SICKNESS RELIEF (MECLIZINE HCL) TABLET, CHEWABLE [PURACAP PHARMACEUTICAL LLC]	1	Current NDC, Legacy NDC, 2 package rows	20171129_8d772ff0-1476-48ca-a7e4-9473ce3db83a.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

Motion Sickness Relief
Meclizine HCl
MECLIZINE HYDROCHLORIDE
MECLIZINE
ASPARTAME
CROSCARMELLOSE SODIUM
DEXTROSE
FD&C RED NO. 40
RASPBERRY
MAGNESIUM STEARATE
MICROCRYSTALLINE CELLULOSE
SUCROSE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
51013-322	51013-322-54

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MECLIZINE HYDROCHLORIDE	HDP7W44CIO	ACTIB
ASPARTAME	Z0H242BBR1	IACT
CROSCARMELLOSE SODIUM	M28OL1HH48	IACT
DEXTROSE	IY9XDZ35W2	IACT
FD&C RED NO. 40	WZB9127XOA	IACT
RASPBERRY	4N14V5R27W	IACT
MAGNESIUM STEARATE	70097M6I30	IACT
MICROCRYSTALLINE CELLULOSE	OP1R32D61U	IACT
SUCROSE	C151H8M554	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
Motion Sickness Relief	MECLIZINE HCL	PuraCap Pharmaceutical LLC	8d772ff0-1476-48ca-a7e4-9473ce3db83a	2017-11-28	Warnings	Exact identifier ndc (package): 51013-322-54 ndc (product): 51013-322 ndc11 (package): 51013032254 spl id: 116d1b6a-03af-4b3c-a81a-e1a598bf4f6b spl set id: 8d772ff0-1476-48ca-a7e4-9473ce3db83a

Reported adverse events (FAERS/openFDA)#

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