Medi-first Non-aspirin Extra Strength Tablet, Film Coated
Product Images NDC 47682-804

3 FDA label images from Unifirst First Aid Corporation · 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 Medi-first Non-aspirin Extra Strength (NDC 47682-804). 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

Mf Non Aspirin Xs Label 12 28 20

Mf Non Aspirin Xs Label 12 28 20
Label for MEDI-FIRST Non-Aspirin Extra Strength 500 mg film-coated tablets, an oral OTC drug containing acetaminophen as the active ingredient. The label highlights its purpose as a pain reliever and fever reducer, for temporary relief of minor aches, pains, and fever. The packaging includes 250 tablets in tamper-evident unit dose packets and is labeled by Unifirst First Aid Corporation. The label also includes bilingual English-Spanish drug facts and usage instructions.*
FDA Label Image

Mfp Non Aspirin Xs Label 12 28 20

Mfp Non Aspirin Xs Label 12 28 20
Packaging label for MEDI-FIRST Non-Aspirin Extra Strength film-coated tablets, containing 500 mg of acetaminophen each. The label shows a red background with white and yellow text, highlighting the product as a pain reliever/fever reducer. It includes a tamper-evident unit dose packet design, and states the package is for households without young children. The labeler is Unifirst First Aid Corporation, with contact information and barcode also visible.*
FDA Label Image

Medique Apapxs Label 12 28 20

Medique Apapxs Label 12 28 20
Packaging label for MEDI-FIRST Non-Aspirin Extra Strength APAP film-coated tablets containing acetaminophen 500 mg. The label highlights the product as a pain reliever and fever reducer, intended for oral use. It features bilingual text in English and Spanish, indicating 250 tablets (125 x 2) in tamper-evident unit dose packets. The labeler is Unifirst First Aid Corporation, with usage and drug facts information included.*

* 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.