Hand Sanitizer
Product Images NDC 75815-521

7 FDA label images from Kb Hps · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 75815-521). 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

355 mL Label (Ndc Ethanol 12 Oz)

355 mL Label (Ndc Ethanol 12 Oz)
Drug Facts panel and front label text for Hand Sanitizer Gel by KB HPS, containing 80% Ethanol Alcohol as the active ingredient. The panel lists inactive ingredients, purpose, uses, warnings, directions, storage, and handling instructions. The front label states the product name, 12 fluid ounce volume, and indicates it is made in the USA.*
FDA Label Image

3785 mL Label (Ndc Ethanol 128 Oz)

3785 mL Label (Ndc Ethanol 128 Oz)
Drug Facts label panel for Hand Sanitizer Gel with 80% ethanol alcohol as the active ingredient. It lists inactive ingredients such as glycerin and hydrogen peroxide, purpose as antiseptic, warnings to avoid heat and for external use only, directions for use, storage instructions, and the manufacturer KB HPS Inc. in Gardena, CA. The label specifies the product volume as 128 fluid ounces (one gallon) and states it is made in the USA.*
FDA Label Image

473 mL Label (Ndc Ethanol 16 Oz)

473 mL Label (Ndc Ethanol 16 Oz)
Drug Facts label for Hand Sanitizer Gel containing 80% Ethanol Alcohol as the active ingredient. Includes inactive ingredients, purpose, uses, warnings, directions, storage and handling information, and manufacturer details from KB HPS, Inc. Made in USA. The label specifies antiseptic use, flammability warning, caution for children, and storage recommendations.*
FDA Label Image

944 mL Label (Ndc Ethanol 32 Oz)

944 mL Label (Ndc Ethanol 32 Oz)
Drug Facts panel for Hand Sanitizer Gel containing 80% ethanol alcohol as the active ingredient, with inactive ingredients including glycerin, purified water USP, hydrogen peroxide, and carbomer. The label details the purpose as an antiseptic hand sanitizer, usage directions, warnings against use on children under 2 months and open wounds, flammability warning, storage instructions, and manufacturer information (KB HPS, Gardena, CA). The front label highlights '80% Alcohol' and 'Hand Sanitizer Gel, 32 FL. OZ., Made in USA.'*
FDA Label Image

118 mL Label (Ndc Ethanol 4 Oz)

118 mL Label (Ndc Ethanol 4 Oz)
Drug Facts panel for a Hand Sanitizer Gel with 80% ethanol alcohol as the active ingredient. Includes inactive ingredients, purpose as an antiseptic hand sanitizer, usage directions, warnings, storage instructions, manufacturer information (KB HPS, Gardena, CA), and product size (4 fl. oz.). Label states Made in USA.*
FDA Label Image

1893 mL Label (Ndc Ethanol 64 Oz)

1893 mL Label (Ndc Ethanol 64 Oz)
Drug Facts panel and front label for Hand Sanitizer Gel by KB HPS featuring 80% Ethanol Alcohol as the active ingredient. The panel includes active and inactive ingredients, purpose as an antiseptic hand sanitizer, usage instructions, warnings, directions, storage instructions, and manufacturer information indicating the product is made in the USA with a volume of 64 fluid ounces.*
FDA Label Image

237 mL 75815-06 (Ndc Ethanol 8 Oz)

237 mL 75815-06 (Ndc Ethanol 8 Oz)
Drug Facts label and front label for Hand Sanitizer Gel containing 80% alcohol. The Drug Facts panel lists active ingredient (80% Ethanol Alcohol), inactive ingredients, purpose, uses, warnings, directions, and storage instructions. The product is made in the USA by KB HPS, INC., Gardena, CA, and is an 8-fluid-ounce container.*

* 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.