Hand Sanitizer
Product Images NDC 78153-000

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 78153-000). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Quimi Clean, 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

Bottle (Bottle)

Hand Sanitizer by Quimi Clean, labeled as a disinfectant with vitamin E and moisturizers, contained in an 8.1 oz (240 ml) bottle. The front label highlights its effectiveness in killing 99.99% of germs in 15 seconds. The back label includes Drug Facts, warnings, and directions for use, noting 70% ethyl alcohol as the active ingredient. The label also states distribution by HB Nutricion in Houston, Texas, USA, and indicates the product is made in Mexico.*

FDA Label Image

Bottle2 (Bottle2)

Hand Sanitizer front and back label from Quimi Clean with 13.5 oz (400 mL) volume. The front states it kills 99.99% of germs in 15 seconds and contains vitamin E and moisturizers. The back includes drug facts listing ethyl alcohol 70% as the active antiseptic ingredient, usage warnings, directions, inactive ingredients, and contact information for Quimi Clean. The product is distributed by HB Nutricion, Houston, Texas, USA.*

FDA Label Image

Bottle3 (Bottle3)

Label of Hand Sanitizer by Quimi Clean showing text in English and Spanish. The label states the product kills 99.99% of germs and contains Vitamin E and moisturizers. It has a volume of 580 ml (19.6 oz). Active ingredient Ethyl Alcohol 70% is indicated, with directions, warnings, and other drug facts included. Distributed by HH Nutricion, Houston, Texas, USA.*

* 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.