DRAMAMINE
- Dosage form
- POWDER
- Labeler
- Medtech Products Inc.
- Label updated
- 2025-12-18
- Retrieved
- 2026-09-07
- Active ingredients
- MECLIZINE DIHYDROCHLORIDE
Label information
Drug Facts
Active ingredient (in each pack )
Meclizine HCl 50 mg
Purpose
Antiemetic
Use
For prevention and treatment of these symptoms associated with motion sickness:
■nausea ■vomiting ■dizziness
Warnings
Do not give to
children under 12 years of age unless directed by a doctor.
Ask a doctor before use if you have
■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
sedatives or tranquilizers.
When using this product
■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,
ask a doctor before use.
Keep out of reach of children .
In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
Directions
■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
■PHENYLKETONURICS: contains phenylalanine 1.68 mg per packet.
■store at room temperature 20°–25°C (68°-77°F)
Inactive i ngredients
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?
1-800-382-7219
Dramamine.com
P RINCIPAL DISPLAY PANEL
Dramamine®
Meclizine Hydrochloride | Antiemetic | 50 mg
Motion Sickness
Less Drowsy Powder
4 Orange Flavored Powder Packs (50 MG EACH)
[Image in the official label — see DailyMed source]
DailyMed Set ID: 6efd3473-ee14-4ee0-8a58-d15a64a9224a · Version 1
NDC: 63029-912