Hand Sanitizer
Product Images NDC 50049-104

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 50049-104). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Quanzhou Besthope Household Products Co.,ltd., 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

1 (8oz 237ml Hand Sanitizer Bottle Upc Rev 9 07052020 01)

1 (8oz 237ml Hand Sanitizer Bottle Upc Rev 9 07052020 01)
This is a drug fact description for a Hand Sanitizer with 75% Ethyl Alcohol (V/V) as an antiseptic ingredient. It is for external use only and is flammable. It should not come in contact with eyes, open skin, or be inhaled or ingested. If skin irritation or redness occurs, stop use and consult a doctor. It should be kept out of reach of children and if swallowed, medical help or Poison Control Center should be contacted. It is not recommended for infants. The product contains 8 FL OZ (237 ml) and includes inactive ingredients such as Acrylates Copolymer, Xanthan gum, Glycerin, Butylene Glycol, Aminomethyl Propanol, and Aloe Barbadensis Leaf Extract. The product is distributed by Sunscope, batch #04/20/2020, and expiration date of 04/19/2022, and made in China.*

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