Medique Medikoff Drops Lozenge
Product Images NDC 47682-050

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Medique Medikoff Drops (NDC 47682-050). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Unifirst First Aid Corporation, 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

050b Mf Cherry (050b Mf Cherry Cough Drops 81525 1 28 21a Label)

MEDI-FIRST Cherry Cough Drops lozenge packaging label showing menthol 7.6 mg as the active ingredient. The label highlights cough suppressant with vapor action, cherry flavor, and individually wrapped lozenges. Includes drug facts, directions, warnings, inactive ingredients, and bilingual information in English and Spanish. Manufactured by Unifirst First Aid Corporation.*

FDA Label Image

Medi-first Plus (Medi First Plus Cherry Cough Drops 91525 1 28 21 Label)

Label for MEDI-FIRST Plus Cherry Cough Drops, menthol 7.6 mg per lozenge, an oral cough suppressant and anesthetic with vapor action. The label is bilingual in English and Spanish, featuring cherry graphics and information for 125 drops per package. Manufactured by Unifirst First Aid Corporation, it includes drug facts, warnings, directions, inactive ingredients, and contact details.*

FDA Label Image

Medique (Medique Medikoff 05022 Rev 1 28 21 Label)

Label for MEDI-FIRST Medikoff Drops, cherry-flavored lozenges containing 7.6 mg menthol per drop. The packaging highlights vapor action and lists menthol as the active ingredient. It is presented as an oral cough suppressant and anesthetic, with 75 drops per container. The labeler is Medique, with directions and drug facts provided in English and Spanish.*

* 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.