Instant Hand Sanitizer
Product Images NDC 73557-230

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Instant Hand Sanitizer (NDC 73557-230). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Shanghai Chuangshi Industry Group 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.

FDA Label Image

73557-230 (73557 230)

Label for INSTANT HAND SANITIZER by Shanghai Chuangshi Industry Group Co., Ltd. It is an antibacterial gel with 75% ethyl alcohol, 1.7 FL OZ (50ML). The front states it kills 99.99% of germs, is safe, quick drying, and used without water. The back includes Drug Facts, directions, warnings, inactive ingredients, manufacturer contact, and barcode.*

FDA Label Image

73557-235 (73557 235)

Label for INSTANT HAND SANITIZER containing 7.6 FL OZ (225 ML) produced by Shanghai Chuangshi Industry Group Co., Ltd. The antibacterial gel contains 75% ethyl alcohol, is for antimicrobial use, and is marketed for killing 99.99% of germs. The label includes usage directions, warnings, and other information such as storage instructions. Contact information and a barcode are also visible.*

FDA Label Image

73557-237 (73557 237)

Label of INSTANT HAND SANITIZER by Shanghai Chuangshi Industry Group Co., Ltd. This antibacterial gel contains 75% ethyl alcohol, is designed for killing 99.99% of germs, and is 11.8 fluid ounces (350 mL) in size. The label highlights its use without water, safe and quick drying properties, and includes drug facts such as active ingredient, warnings, directions, and inactive ingredients like water, glycerin, carbomer, and fragrance.*

* 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.