Dramamine Chewable Orange Tablet, Chewable
Product Images NDC 63029-915

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Dramamine Chewable Orange (NDC 63029-915). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medtech Products Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Principal Display Paneldramamine®meclizine Hydrochloride | Antiemetic | 25 mgmotion Sicknesschewabledual Action:prevents & Relieves Nausea,dizziness And Vomiting8 Orange-flavored Chewable Tablets (Dramamine Chewable Orange Meclizine 63029 915 01)

Dramamine Chewable Orange tablets packaging label showing 25 mg meclizine hydrochloride chewable tablets for motion sickness. Label highlights dual action for preventing and relieving nausea, dizziness, and vomiting. The package includes 8 orange-flavored chewable tablets by Medtech Products Inc. Prominent text notes it is the #1 pharmacist-recommended brand and now contains meclizine.*

FDA Label Image

Principal Display Paneldramamine®meclizine Hydrochloride | Antiemetic | 25 mgmotion Sicknesschewabledual Action:prevents & Relieves Nausea,dizziness And Vomiting8 Orange-flavored Chewable Tablets (Dramamine Chewable Orange Meclizine 63029 915 02)

Drug Facts panel for DRAMAMINE CHEWABLE ORANGE 25 mg Meclizine Hydrochloride chewable tablets by Medtech Products Inc. The panel includes active ingredient, uses, warnings, directions, inactive ingredients, and contact information for questions or comments. It covers usage instructions, precautions, and storage guidance for this oral over-the-counter medication.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.