Wolke Hand Sanitizer
Product Images NDC 78207-000

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Wolke Hand Sanitizer (NDC 78207-000). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hidro Soluciones Integrales, S.a. De C.v., 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)

Drug Facts label for Wolke Hand Sanitizer shows active ingredient as Alcohol 70% v/v with antiseptic purpose. It includes usage instructions, warnings for external use, flammability warnings, guidance to keep out of reach of children, directions for use, and other storage information. Inactive ingredients listed are purified water, carbomer, triethanolamine, and glycerin. The label notes the product is made in Mexico and distributed by Hidro Soluciones Integrales S.A. de C.V.*

FDA Label Image

Bottle2 (Bottle2)

Wolke Hand Sanitizer moisturizing gel with 70% alcohol, in a 16.9 FL. OZ (500 ml) bottle by Hidro Soluciones Integrales, S.A. de C.V. The label highlights its germ-killing efficacy and includes Drug Facts with active ingredient, uses, warnings, directions, and inactive ingredients. The product is made in Mexico.*

FDA Label Image

Bottle3 (Bottle3)

Wolke Hand Sanitizer moisturizing gel with 70% alcohol strength in a 30.4 FL. OZ (900 ml) bottle. The label features the Wolke logo and claims to kill 99.99% of germs. It is distributed by Hidro Soluciones Integrales S.A. de C.V., made in Mexico, and includes basic drug facts and usage warnings on the label's right side.*

* 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.