Alcohol Prep Pads Swab
Product Images NDC 60913-048

View Photos of 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 Alcohol Prep Pads (NDC 60913-048). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Phoenix Healthcare Solutions Llc, 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

Acme 10ct (10ct)

Acme 10ct (10ct)
Packaging label for First Aid Only Alcohol Antiseptic Pads containing 10 wipes. The active ingredient is Isopropyl Alcohol 70%, with purified water as inactive ingredient. The label includes warnings, directions, and storage information. Manufactured for Acme United Corporation and made in India.*
FDA Label Image

Acme 20ct (20ct)

Acme 20ct (20ct)
The packaging label is for Alcohol Antiseptic Pads, containing 20 wipes. The front panel shows the product name with the First Aid Only brand and a barcode. The side panel includes SmartTab First Aid ezRefill System instructions. The drug facts panel lists Isopropyl Alcohol 70% as the active ingredient, with details on use, warnings, directions, and storage. Manufacturer listed as Acme United Corporation, made in India.*
FDA Label Image

Acme 50ct (50ct)

Acme 50ct (50ct)
Drug Facts panel for alcohol antiseptic pads containing 70% isopropyl alcohol as the active ingredient. Includes warnings for external use only, flammability, and directions to wipe injection site vigorously and discard. Additional information notes product sterility unless pouch is opened or damaged, storage recommendations, and purified water as the inactive 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.