Dramamine Original Formula Tablet
Product Images NDC 63029-901

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Dramamine Original Formula (NDC 63029-901). 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 Paneldimenhydrinate Tablets/antiemeticoriginal Formula Dramamine36 Tablets (50 mg Each) (Dramamine Original Formula 01)

Principal Display Paneldimenhydrinate Tablets/antiemeticoriginal Formula Dramamine36 Tablets (50 mg Each) (Dramamine Original Formula 01)
Label for Dramamine Original Formula dimenhydrinate 50 mg oral tablets, packaged by Medtech Products Inc. The label features motion sickness relief claims and highlights dual action for treating symptoms and preventing nausea, dizziness, and vomiting. It includes a depiction of a single tablet, dosage strength, and a 12 tablet count per package, along with drug facts and usage instructions.*
FDA Label Image

Dramamine Original Formula 02

Dramamine Original Formula 02
Packaging label for Dramamine Original Formula 50 mg tablets by Medtech Products Inc. The box is predominantly yellow with blue and red accents, featuring the brand name and product purpose as motion sickness relief. It contains 36 tablets and highlights treatment for nausea, dizziness, and vomiting symptoms.*

* 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.