Severe Throat Sore Drops Pastille
Product Images NDC 11673-143

2 FDA label images from Target Corporation Inc. · 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 Severe Throat Sore Drops (NDC 11673-143). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Target Corporation 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

Back Label (20191014 Target Sever Cough Drop 45ct Bag File Back)

Back Label (20191014 Target Sever Cough Drop 45ct   Bag File    Back)
Drug Facts panel for Severe Throat Sore Drops pastilles, containing 20 mg Menthol as the active ingredient. The panel includes uses, warnings, directions for adults and children, inactive ingredients, storage instructions, and a contact number for questions or adverse event reporting. Additional labeling notes distributor Target Corporation, product origin Spain, and trademark information.*
FDA Label Image

Front Label (20191014 Target Sever Cough Drop 45ct Bag File Front)

Front Label (20191014 Target Sever Cough Drop 45ct   Bag File    Front)
Packaging label for Severe Throat Drops oral anesthetic pastilles with menthol, by Target Corporation under the up&up brand. The reclosable bag contains 45 menthol ice flavored drops with maximum strength menthol for soothing severe sore throat pain. The label highlights comparison to Vicks Severe VapoCool active ingredient.*

* 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.