Pepto MOTION SICKNESS

Manufacturer: THE PROCTER & GAMBLE MANUFACTURING COMPANY
Effective date: 2026-10-05
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: daily-update
Hydrated at: 2026-10-09 01:01:13

Label at a glance#

ProductPepto Motion Sickness

Active ingredientMECLIZINE HYDROCHLORIDE

Label structure12 sections

Indications and uses

for the prevention and treatment of nausea, vomiting, or dizziness associated with motion sickness

Dosage and administration

take ½ to 1 hour before traveling adults and children 12 years and over: 1 to 2 tablets once daily or as directed by a doctor

Contacts and useful links#

PhoneLabel contact1-800-717-3786

Label contents#

Full prescribing information#

Pepto MOTION SICKNESS

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient (in each tablet)

OTC - ACTIVE INGREDIENT SECTION

Meclizine HCl 25 mg

Purpose

OTC - PURPOSE SECTION

Antiemetic

Uses

INDICATIONS & USAGE SECTION

for the prevention and treatment of nausea, vomiting, or dizziness associated with motion sickness

Warnings

WARNINGS SECTION

Do not use

OTC - DO NOT USE SECTION

in 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
difficulty in urination due to enlargement of the 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
use caution when driving a motor vehicle or operating machinery

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

OVERDOSAGE SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

take ½ to 1 hour before traveling
adults and children 12 years and over: 1 to 2 tablets once daily or as directed by a doctor

Other information

SPL UNCLASSIFIED SECTION

Store at room temperature 20°-25°C (68°-77°F).

INACTIVE INGREDIENT SECTION

anhydrous lactose, corn starch, FD&C Red No. 40 Aluminum Lake, magnesium stearate, microcrystalline cellulose, silicon dioxide

Questions?

OTC - QUESTIONS SECTION

1-800-717-3786

SPL UNCLASSIFIED SECTION

TAMPER EVIDENT: CARTON SEALED FOR YOUR
PROTECTION. DO NOT USE IF CARTON IS OPENED OR TORN.
IMPORTANT: KEEP CARTON FOR FUTURE REFERENCE.

SPL UNCLASSIFIED SECTION

DIST. BY: PROCTER &

GAMBLE, CINCINNATI, OH

45202

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Meclizine HCl -
Antiemetic

Pepto

Motion

Sickness

TARGETED NAUSEA RELIEF

PREVENTS + RELIEVES NAUSEA

LESS DROWSY

10 TABLETS

380

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0301490003732	GTIN-13: 0301490003732 EAN-13: 0301490003732 GTIN-12: 301490003732 UPC-A: 301490003732 GTIN storage (14 digits): 00301490003732	380.jpg
QR code link	QR Code	scan.pg.com/01/00301490003732		380.jpg
Data code	Data Matrix	21442228		380.jpg

Products#

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

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

Pepto Motion Sickness
Meclizine HCl
MECLIZINE HYDROCHLORIDE
MECLIZINE
ANHYDROUS LACTOSE
STARCH, CORN
FD&C RED NO. 40 ALUMINUM LAKE
MAGNESIUM STEARATE
MICROCRYSTALLINE CELLULOSE
SILICON DIOXIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
84126-380	84126-380-01, 84126-380-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MECLIZINE HYDROCHLORIDE	HDP7W44CIO	ACTIB
ANHYDROUS LACTOSE	3SY5LH9PMK	IACT
STARCH, CORN	O8232NY3SJ	IACT
FD&C RED NO. 40 ALUMINUM LAKE	6T47AS764T	IACT
MAGNESIUM STEARATE	70097M6I30	IACT
MICROCRYSTALLINE CELLULOSE	OP1R32D61U	IACT
SILICON DIOXIDE	ETJ7Z6XBU4	IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
1	2026-07-21	daily-update	2026-09-03 03:01:47

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
571e3eeb-ae9f-7054-e063-6394a90a2634			571e3eeb-ae9e-7054-e063-6394a90a2634	2026-07-21	Warnings	Exact identifier spl set id: 571e3eeb-ae9e-7054-e063-6394a90a2634

Reported adverse events (FAERS/openFDA)#

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