Dramamine Less Drowsy

Manufacturer: Navajo Manufacturing Company Inc.
Effective date: 2026-02-18
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 01:46:36

Label at a glance#

ProductDramamine Less Drowsy

Active ingredientMECLIZINE HYDROCHLORIDE

Label structure10 sections

Dosage and administration

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

Contacts and useful links#

PhonePoison Help1-800-222-1222

PhoneLabel contact1-800-382-7219

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

(in each tablet)

Meclizine HCI 25 mg

Purpose

OTC - PURPOSE SECTION

Antiemetic

Use

INDICATIONS & USAGE SECTION

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

nausea
vomiting
dizziness

Warnings

WARNINGS SECTION

Do notgive

OTC - DO NOT USE SECTION

to 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 aretaking

OTC - ASK DOCTOR/PHARMACIST SECTION

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 1/2 to 1 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

OTHER SAFETY INFORMATION

store at room temperature 20 - 25 ^ºC (68 - 77 ^ºF)

Inactive ingredients

INACTIVE INGREDIENT SECTION

anhydrous lactose, corn starch, colloidal silicon dioxide, D&C yellow no. 10 aluminum lake, magnesium stearate, microcrystalline cellulose

Questions?

OTC - QUESTIONS SECTION

1-800-382-7219

Dramamine.com

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dramamine

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
995726	Dramamine Less Drowsy 25 MG Oral Tablet	PSN	1
995666	meclizine HCl 25 MG Oral Tablet	PSN	1
995726	meclizine hydrochloride 25 MG Oral Tablet [Dramamine Less Drowsy]	SBD	1
995666	meclizine hydrochloride 25 MG Oral Tablet	SCD	1
995726	Dramamine II 25 MG Oral Tablet	SY	1
995726	Dramamine Less Drowsy 25 MG Oral Tablet	SY	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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
67751-242-02	Dramamine Less Drowsy	1 in 1 CARTON	TABLET	1	1
67751-242-02	Dramamine Less Drowsy	2 in 1 POUCH	TABLET	2	1
67751-242-04	Dramamine Less Drowsy	2 in 1 CARTON	TABLET	2	1
67751-242-04	Dramamine Less Drowsy	2 in 1 POUCH	TABLET	2	1

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

Dramamine Less Drowsy
Meclizine Hydrochloride
ANHYDROUS LACTOSE
STARCH, CORN
SILICON DIOXIDE
D&C YELLOW NO. 10
MAGNESIUM STEARATE
CELLULOSE, MICROCRYSTALLINE
MECLIZINE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
67751-242	67751-242-02, 67751-242-04
63029-903

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
ANHYDROUS LACTOSE	3SY5LH9PMK	IACT
STARCH, CORN	O8232NY3SJ	IACT
SILICON DIOXIDE	ETJ7Z6XBU4	IACT
D&C YELLOW NO. 10	35SW5USQ3G	IACT
MAGNESIUM STEARATE	70097M6I30	IACT
CELLULOSE, MICROCRYSTALLINE	OP1R32D61U	IACT
MECLIZINE HYDROCHLORIDE	HDP7W44CIO	ACTIB

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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Dramamine Less Drowsy	MECLIZINE HYDROCHLORIDE	Medtech Products Inc.	fa6a0969-7427-4b87-bc04-a2792665c218	2026-09-04	Warnings	Exact identifier ndc (product): 63029-903
Dramamine Less Drowsy	MECLIZINE HYDROCHLORIDE	Navajo Manufacturing Company Inc.	4b203479-ba8d-7237-e063-6294a90ae6cb	2026-02-18	Warnings	Exact identifier ndc (package): 67751-242-04 ndc (package): 67751-242-02 ndc (product): 67751-242 ndc11 (package): 67751024202 ndc11 (package): 67751024204 spl id: 4b20367a-2f77-74e8-e063-6294a90a4855 spl set id: 4b203479-ba8d-7237-e063-6294a90ae6cb

Reported adverse events (FAERS/openFDA)#

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