No Touch Chest Rub
Product Images NDC 41250-702

3 FDA label images from Meijer · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for No Touch Chest Rub (NDC 41250-702). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Meijer, 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

Image Description (Back 1)

Image Description (Back 1)
Drug Facts panel for No Touch Chest Rub by Meijer. Lists active ingredients including Camphor 4.8%, Eucalyptus Globulus Leaf Oil 1.2%, and Menthol 2.6%, all labeled as cough suppressant and topical analgesic. States uses for temporary relief of cough due to common cold and minor aches. Includes a warning for external use only and to avoid eye contact. Distributor information and barcode are shown below.*
FDA Label Image

Image Description (Back 2)

Image Description (Back 2)
This Drug Facts panel for No Touch Chest Rub includes warnings against use by mouth, on wounds or damaged skin, and with tight bandages or in nostrils. It advises consulting a doctor for certain coughs and provides directions for use, including application instructions and age restrictions. The panel also lists inactive ingredients such as beeswax and mineral oil, and storage information.*
FDA Label Image

Image Description (Front)

Image Description (Front)
No Touch Chest Rub medicated topical product by Meijer, labeled with active ingredients camphor 4.8%, menthol 2.6%, and eucalyptus globulus leaf oil 1.2%. The net weight is 1.5 ounces (43 grams). The label compares it to Vick's VapoRub and highlights convenient application for relief of cough and minor muscle ache.*

* 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.