Gnc Instant Hand Sanitizer
Product Images NDC 43655-1111

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Gnc Instant Hand Sanitizer (NDC 43655-1111). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gnc Holdings 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

Principal Display Panel (118 mL Bottle Label)

This is a hand sanitizer that contains 66.5% of Ethyl Alcohol, with a fresh scent. It is intended for external use only and recommended for repeated use to help reduce bacteria on hands and skin. It comes in a bottle size of 118 ml and has directions for usage, which includes wetting the hands thoroughly with the product and allowing them to dry without wiping. It also has a list of inactive ingredients, and a warning list that includes keeping it away from children, not using it in the eyes, and seeking a doctor's help if redness or irritation develops. The product has been distributed by GNC Holdings, LLC, and more information can be obtained through their customer service number.*

FDA Label Image

Principal Display Panel (237 mL Bottle Label)

This is a drug fact description for a hand sanitizer. Its active ingredient is ethyl alcohol 66.5%, and it is used as an antiseptic to help reduce bacteria on hands and skin. It is not recommended for use in the eyes and should be kept away from fire or flames. In case of irritation, redness, or ingestion, one should seek medical help. The product contains purified water, carbomer, aloe vera, and other ingredients and comes in a fresh scent. It is distributed by GC Holdings L, and it weighs 8.0 FL OZ. (237mL).*

* 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.