Hand Sanitizer
Product Images NDC 75280-802

8 FDA label images from Frank-lin Distillers Products, Ltd. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 75280-802). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Frank-lin Distillers Products, 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.

FDA Label Image

1750 mL Back (Jezero 1750 mL Back)

1750 mL Back (Jezero 1750 mL Back)
Drug Facts panel for Hand Sanitizer by Frank-Lin Distillers Products, Ltd. The active ingredient is Alcohol 80% v/v serving as an antiseptic. It includes uses, warnings, directions, and storage information. Volume is 1.75 L (59.2 fl. oz). The product is made in the USA and contains inactive ingredients glycerin, hydrogen peroxide, and purified water USP.*
FDA Label Image

1750 mL Front (Jezero 1750 mL Front)

1750 mL Front (Jezero 1750 mL Front)
Label for JEZERO Hand Sanitizer, a non-sterile solution. The product is an alcohol antiseptic 80% topical solution in a 1.75 L (59.2 FL. OZ.) container. The label features the JEZERO logo prominently at the top and includes the product name and description with a light blue patterned border.*
FDA Label Image

200 mL Back (Jezero 200 mL Back)

200 mL Back (Jezero 200 mL Back)
Drug Facts panel for Hand Sanitizer by Frank-Lin Distillers Products, Ltd. The panel lists active ingredient as Alcohol 80% v/v with antiseptic purpose. It includes uses, warnings, directions, storage information, and inactive ingredients (glycerin, hydrogen peroxide, purified water USP). The product volume is 200 ml (6.7 fl. oz.) and is made in the USA.*
FDA Label Image

200 mL Ndc: 75280-802-01 (Jezero 200 mL Front)

200 mL Ndc: 75280-802-01 (Jezero 200 mL Front)
JEZERO Hand Sanitizer label for a non-sterile solution containing 80% alcohol antiseptic. The label displays the product name prominently with volume listed as 200 ml (6.7 FL. OZ.). The labeler is Frank-Lin Distillers Products, Ltd.*
FDA Label Image

375 mL Back (Jezero 375 mL Back)

375 mL Back (Jezero 375 mL Back)
Drug Facts label for Hand Sanitizer by Frank-Lin Distillers Products, Ltd. Lists active ingredient as alcohol 80% v/v with antiseptic purpose. Includes warnings for external use only, flammability, and safe usage instructions. Directions recommend applying enough product to cover hands and supervising children under 6. Storage instructions and inactive ingredients (glycerin, hydrogen peroxide, purified water USP) are noted. Label states 375 ml (12.7 fl. oz.) volume and made in the USA.*
FDA Label Image

375 mL Front (Jezero 375 mL Front)

375 mL Front (Jezero 375 mL Front)
Packaging label for JEZERO Hand Sanitizer, a non-sterile alcohol antiseptic topical solution with 80% concentration. The label indicates a volume of 375 ml (12.7 FL. OZ.) and is produced by Frank-Lin Distillers Products, Ltd.*
FDA Label Image

750 mL Back (Jezero 750 mL Back)

750 mL Back (Jezero 750 mL Back)
Drug Facts label for Hand Sanitizer produced by Frank-Lin Distillers Products, Ltd. Lists active ingredient as Alcohol 80% v/v with an antiseptic purpose. Includes usage directions, warnings, storage instructions, and inactive ingredients (glycerin, hydrogen peroxide, purified water USP). Volume is 750 ml (25.4 fl. oz) and the product is made in the USA.*
FDA Label Image

750 mL Front (Jezero 750 mL Front)

750 mL Front (Jezero 750 mL Front)
The label for Jezero Hand Sanitizer, a non-sterile topical solution containing 80% alcohol antiseptic. The label states the volume as 750 ml (25.4 FL. OZ.) and features the brand name Jezero prominently at the top. The product is labeled as a hand sanitizer solution.*

* 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.