Hand Sanitizer
Product Images NDC 76782-003

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 76782-003). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Blue Mineral 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.

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FDA Label Image

Label (Label 1)

Label (Label 1)
This is a drug fact label for a hand sanitizer. The active ingredient is ethyl alcohol 75%, which helps to decrease bacteria on the skin. It is recommended for repeated use. The label warns that the product is for external use only, and to avoid contact with the eyes. If irritation or redness develops or persists for more than 72 hours, or if swallowed, get medical help or contact a Poison Control Center right away. To use, squeeze an appropriate amount of sanitizer onto hands and rub together until dry. The inactive ingredients are water, aloe barbadensis leaf extract, acrylates/C10-30 alkyl acrylate crosspolymer, and tetrahydroxypropyl ethylenediamine. The label also includes information on the hygiene license of the production enterprise and executive standard. The product comes in a bottle with a volume of 8.45 FL.OZ and an expiration date of 03/2022.*

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