Hand Sanitizer
Product Images NDC 75815-916

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 75815-916). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Kb Hps, 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

355ml Label (Ndc Isopropyl 12 Oz)

Drug Facts label for Hand Sanitizer Gel containing 75% isopropyl alcohol as the active ingredient. It includes inactive ingredients such as glycerin, purified water USP, hydrogen peroxide, and carbomer. The label provides warnings about flammability and use instructions, directions for application, storage conditions, and manufacturer information (KB HPS, Gardena, CA). The front label shows the product name, 75% alcohol content, and volume of 12 fluid ounces, noting it is made in the USA.*

FDA Label Image

3785 mL Label (Ndc Isopropyl 128 Oz)

Drug Facts panel for Hand Sanitizer Gel, listing active ingredient as 75% isopropyl alcohol. It includes inactive ingredients, purpose as antiseptic hand sanitizer, uses, warnings, directions, and storage information. The label notes the product is made in the USA by KB HPS, Inc., Gardena, CA, with a NDC of 75815-916-15. The front label states the product contains 128 fluid ounces (one gallon) and emphasizes 75% alcohol content.*

FDA Label Image

473ml Label (Ndc Isopropyl 16 Oz)

Drug Facts panel and front label of Hand Sanitizer Gel containing 75% isopropyl alcohol. The Drug Facts list active and inactive ingredients, purpose, uses, warnings, directions, and storage instructions. The label indicates the product is 16 fluid ounces, made in the USA, and manufactured by KB HPS, Inc., Gardena, CA.*

FDA Label Image

59ml Label (Ndc Isopropyl 2 Oz)

Hand Sanitizer Gel 2 FL. OZ. label from KB HPS features 75% Alcohol as the active ingredient. The label includes drug facts, warnings, directions, and storage information, with manufacturing details showing it is made in the USA by KB HPS, Inc., Gardena, CA.*

FDA Label Image

946ml Label (Ndc Isopropyl 32 Oz)

Drug Facts panel and front label of Hand Sanitizer Gel with 75% isopropyl alcohol, 32 FL. OZ. The label includes active ingredients, purpose, uses, warnings, directions, storage instructions, and manufacturing information by KB HPS, Gardena, CA. It states the product is made in the USA.*

FDA Label Image

118 mL Label (Ndc Isopropyl 4 Oz)

Drug Facts panel and label for Hand Sanitizer Gel containing 75% isopropyl alcohol as the active ingredient. The panel lists inactive ingredients, purpose, uses, warnings, directions, and storage instructions. The label states the product volume as 4 FL. OZ. and notes it is made in the USA by KB HPS, Inc., Gardena, CA.*

FDA Label Image

1893 mL Label (Ndc Isopropyl 64 Oz)

Drug Facts label for Hand Sanitizer Gel with 75% Isopropyl Alcohol as the active ingredient. The panel lists inactive ingredients, purpose, uses, warnings including flammability, do not use instructions, directions for use, storage and handling guidelines. It also states the product is made in the USA by KB HPS, Inc., Gardena, CA, with NDC 75815-916-13. The front panel indicates the product is Hand Sanitizer Gel, 64 FL. OZ., with 75% alcohol content.*

FDA Label Image

237ml Ndc: 75815-916-05 (Ndc Isopropyl 8 Oz)

Drug Facts panel for Hand Sanitizer Gel showing active ingredient as 75% Isopropyl Alcohol. It lists inactive ingredients including glycerin, purified water USP, hydrogen peroxide, and carbomer. The label includes purpose, uses, warnings, directions, and storage instructions. The product is manufactured by KB HPS, Inc. in Gardena, CA.*

* 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.