DRAMAMINE

Manufacturer: Medtech Products Inc.
Effective date: 2025-12-18
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 01:36:06

Label at a glance#

ProductDRAMAMINE

Active ingredientMECLIZINE DIHYDROCHLORIDE

Label structure10 sections

Dosage and administration

■take dose ½ to 1 hour before starting activity ■ adults and children 12 years and over: place 1 packet on tongue 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 (in each pack)

OTC - ACTIVE INGREDIENT SECTION

Meclizine HCl 50 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 not give to

OTC - DO NOT USE SECTION

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 taking

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 dose ½ to 1 hour before starting activity

■adults and children 12 years and over: place 1 packet on tongue once daily, or as directed by a doctor

Other information

OTHER SAFETY INFORMATION

■PHENYLKETONURICS: contains phenylalanine 1.68 mg per packet.

■store at room temperature 20°–25°C (68°-77°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

anhydrous citric acid, ascorbic acid, aspartame, butylated hydroxytoluene, corn starch, guar gum, maltodextrin, mannitol, microcrystalline cellulose, natural orange flavor, natural pink lemonade flavor, silicon dioxide, sorbitol.

Questions?

OTC - QUESTIONS SECTION

1-800-382-7219

Dramamine.com

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dramamine®

Meclizine Hydrochloride | Antiemetic | 50 mg

Motion Sickness

Less Drowsy Powder

4 Orange Flavored Powder Packs (50 MG EACH)

Dramamine® Meclizine Hydrochloride | Antiemetic | 50 mg Motion Sickness Less Drowsy Powder 4 Orange Flavored Powder Packs (50 MG EACH)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2734137	Dramamine Less Drowsy 50 MG Oral Powder	PSN	1
2734132	meclizine hydrochloride 50 MG Oral Powder	PSN	1
2734137	meclizine hydrochloride 50 MG Oral Powder [Dramamine Less Drowsy]	SBD	1
2734132	meclizine hydrochloride 50 MG Oral Powder	SCD	1
2734137	Dramamine Less Drowsy 50 MG Oral Powder	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
c5cd4727-ac49-4409-82b1-5bd8006c3ec7	Product name	1	20171122

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63029-912-04	DRAMAMINE	4 in 1 BOX	POWDER	4		1

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

DRAMAMINE
MECLIZINE HYDROCHLORIDE
MECLIZINE DIHYDROCHLORIDE
MECLIZINE
ANHYDROUS CITRIC ACID
ASCORBIC ACID
ASPARTAME
BUTYLATED HYDROXYTOLUENE
STARCH, CORN
GUAR GUM
MALTODEXTRIN
MANNITOL
MICROCRYSTALLINE CELLULOSE
SILICON DIOXIDE
SORBITOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
63029-912	63029-912-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MECLIZINE DIHYDROCHLORIDE	HDP7W44CIO	ACTIB
ANHYDROUS CITRIC ACID	XF417D3PSL	IACT
ASCORBIC ACID	PQ6CK8PD0R	IACT
ASPARTAME	Z0H242BBR1	IACT
BUTYLATED HYDROXYTOLUENE	1P9D0Z171K	IACT
STARCH, CORN	O8232NY3SJ	IACT
GUAR GUM	E89I1637KE	IACT
MALTODEXTRIN	7CVR7L4A2D	IACT
MANNITOL	3OWL53L36A	IACT
MICROCRYSTALLINE CELLULOSE	OP1R32D61U	IACT
SILICON DIOXIDE	ETJ7Z6XBU4	IACT
SORBITOL	506T60A25R	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
DRAMAMINE	MECLIZINE HYDROCHLORIDE	Medtech Products Inc.	6efd3473-ee14-4ee0-8a58-d15a64a9224a	2025-12-18	Warnings	Exact identifier ndc (package): 63029-912-04 ndc (product): 63029-912 ndc11 (package): 63029091204 spl id: 871f81c0-8d71-4ff5-8317-9a1f74ba7b83 spl set id: 6efd3473-ee14-4ee0-8a58-d15a64a9224a

Reported adverse events (FAERS/openFDA)#

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