Hand Sanitizer
Product Images NDC 75628-001

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 75628-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Tommyrotter Distillery, 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

3785.ml Label (3785.41 mL Label)

3785.ml Label (3785.41 mL Label)
This is a non-sterile Hand Sanitizer manufactured by Tommyrotter Distillery. The solution is a topical alcohol antiseptic with 80% strength, made under emergency measures by WHO & FDA formulation. This product helps to reduce bacteria that potentially can cause disease when soap and water are not available. The solution is in a 1-gallon container with drug facts, directions, and warnings printed on the label. It is for external use only and should be kept away from children, eyes, ears, and mouth, and should not be used in children less than 2 months of age or on open skin wounds. If swallowed, get medical help right away. The only active ingredient in this product is alcohol, and it comes with inactive ingredients like glycerin, hydrogen peroxide, and purified water USP. It requires storage between 15-30C and should avoid freezing and excessive heat.*

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