Hand Sanitizer
Product Images NDC 76933-001

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 76933-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bee Sales Co., 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

Hand Sanitizer 100 mL (Sanitizer 100ml)

HAND SANITIZER Gel 100 ml packaging label from BEE SALES CO. The label details the active ingredient, isopropyl alcohol at 75%, as a topical antiseptic solution. It includes drug facts such as uses, warnings, directions, and inactive ingredients. The product is a non-sterile hand sanitizer gel distributed by BEE SALES CO., made in P.R.C. The sticker dimensions for front and back labels are shown.*

FDA Label Image

Hand Sanitizer 500 mL (Sanitizer 500ml)

Sticker labels for HAND SANITIZER GEL 500ml by BEE SALES CO. The front label highlights Isopropyl Alcohol Antiseptic 75% as the active ingredient and states it is a non-sterile topical solution. The back label provides detailed Drug Facts including purpose, use, warnings, directions, other information, and inactive ingredients. The product is distributed by BEE SALES CO., Niles, IL, made in P.R.C.*

FDA Label Image

60ml Hand Sanitizer (Sanitizer 60ml)

Label of Hand Sanitizer Gel 60ml by Bee Sales Co. featuring the active ingredient Isopropyl Alcohol Antiseptic at 75%. It is a non-sterile topical solution with packaging sizes noted, featuring Drug Facts including warnings, directions, and inactive ingredients such as glycerin, hydrogen peroxide, and purified water USP. Distributed by Bee Sales Co. in Niles, IL, made in P.R.C.*

* 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.