Dramamine Less Drowsy Meclizine Hydrochloride Tablet
Product Images NDC 50269-526

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 Less Drowsy Meclizine Hydrochloride (NDC 50269-526). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Jc World Bell Wholesale Co., 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

Inner Label 3 (Inner Label 3)

Inner Label 3 (Inner Label 3)
Labels for Dramamine Less Drowsy Meclizine Hydrochloride 25 mg tablets show branding, motion sickness indication, and a count of 2 tablets. Active ingredient is Meclizine HCl 25 mg per tablet, used as an antiemetic. Directions state to take the first dose ½ to 1 hour before activity, with dosing for adults and children 12 years and over as 1 to 2 tablets once daily or as directed by a doctor. Storage instructions specify room temperature and not to use if pouch is opened. Distributor information is also included.*
FDA Label Image

Outer Label3 (Outer Label3)

Outer Label3 (Outer Label3)
Packaging label for Dramamine Less Drowsy Meclizine Hydrochloride 25 mg tablet by JC World Bell Wholesale Co., Inc. The yellow box features the brand name Dramamine prominently with antihistamine and antiemetic properties indicated. The label highlights it is for motion sickness with less drowsiness. Dosage instructions, drug facts, warnings, and manufacturer details appear on the side panel. The package contains 20 packets of 2 tablets each.*

* 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.