Afia Alcohol-free Foaming Hand Sanitizer (Fda Ncl Hand Sanitizer Submission Carton Compressed 101016)
Afia Alcohol-free Foaming Hand Sanitizer
Product Images NDC 71023-445
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Product Visual Gallery
This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Afia Alcohol-free Foaming Hand Sanitizer (NDC 71023-445). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by National Chemical Laboratories, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Active Ingredient. Purpose Benzalkonium Chloride 0.1%...........antimicrobial (Fda Ncl Hand Sanitizer Submission Label 101016)
This is a drug facts label for a foaming hand sanitizer produced by National Chemical Laboratories, Inc. The active ingredient is benzalkonium chloride 0.1%, which serves as an antimicrobial to reduce bacteria on the skin. The product is recommended for repeated use but should only be used externally. It comes in a 1000 ml container and is alcohol-free. Other ingredients include water, glycereth-2 cocoate, behentrimonium chloride, and fragrance. If the product causes irritation or redness, users should discontinue use and consult a doctor. Children should be kept away from the product, and if swallowed, medical attention should be sought immediately. The product is applied by pumping a small amount of foam in one’s palm and rubbing the hands together briskly until dry.*
Afia Alcohol-free Foaming Hand Sanitizer (Fda Ncl Hand Sanitizer Submission Package Picture Compressed 101016)
* 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.
