Isopropyl Alcohol
Product Images NDC 49348-896

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Isopropyl Alcohol (NDC 49348-896). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Strategic Sourcing Services 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

125 7104 Box

125 7104 Box
This is a drug fact sheet for Sunmark Sterile Alcohol packaged as 100 individual foil packets. The active ingredient in this product is Isopropyl Alcohol which is used to clean the skin before the injection while the inactive ingredient is purified water. The product should be used externally only and kept away from fire or flame. The user must seek medical attention if swallowed and stop using if redness or irritation develops. The product should be applied to the intended area and then discarded after use. This product is manufactured in China and distributed by McKesson located in San Francisco.*
FDA Label Image

125 7104 Case

125 7104 Case
This is a product description for sterile alcohol prep pads manufactured by "Sunmark" brand. The pad contains 70% isopropyl alcohol and each case contains 20 boxes. The product is distributed by McKesson and made in China. The mentioned lot number is "09913" and the address of the distributor is One Post Street, San Francisco, CA 94104.*
FDA Label Image

125 7104 Each

125 7104 Each
This is a Sunmark Sterile Alcohol Prep Pad containing 1 pad, which is made in China and distributed by McKesson from San Francisco, CA. It serves as an antiseptic for the preparation of the skin before injection, and it has a 70% isopropyl alcohol solution. The product label includes a Money-Back Guarantee, but it also warns that it is flammable and should be kept away from fire or flame. The instructions for use specify that the pad should be discarded after a single use, and that it should not be used with electrocautery or in the eyes. If redness or irritation develops, the use should be stopped and a physician must be consulted if the condition persists for more than 72 hours. The inactive ingredients include 30% purified water. The text also displays a lot number and an expiration date, but without clear recognition.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.