Medi-first Cherry Cough Drops Lozenge
Product Images NDC 47682-815

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Medi-first Cherry Cough Drops (NDC 47682-815). 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

Medi First Cherry Cough Drops 81525 1 28 21 Label

The packaging label for MEDI-FIRST Cherry Cough Drops features a red and white design with cherries graphics. The product is a lozenge containing 7.6 mg of menthol per dose, used as a cough suppressant with vapor action. The package states the lozenges are individually wrapped and includes the labeler information: Unifirst First Aid Corporation. Directions, warnings, and Drug Facts are displayed in English and Spanish.*

FDA Label Image

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 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.