Foaming Instant Hand Sanitizer With Aloe And Vitamin E
Product Images NDC 50865-207

6 FDA label images from Kutol Products Company, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Foaming Instant Hand Sanitizer With Aloe And Vitamin E (NDC 50865-207). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Kutol Products Company, Inc., 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

Foaming Instant 532 mL (68217 Ez Foamhh 1 7 Insthandsan207 Laxxx 1215)

Foaming Instant 532 mL (68217 Ez Foamhh 1 7 Insthandsan207 Laxxx 1215)
Label for Foaming Instant Hand Sanitizer with Aloe and Vitamin E by Kutol Products Company. The label highlights it as an instant hand sanitizer for use without water, containing no alcohol. The product comes in a 50 mL (1.7 fl. oz.) size. The label includes Drug Facts with active ingredient Benzalkonium Chloride 0.13%, usage instructions, warnings, and a list of inactive ingredients.*
FDA Label Image

Foaming Instant 1000 mL (68241 Foaming Bag Hand Sannoalc207 Laxxx 1215)

Foaming Instant 1000 mL (68241 Foaming Bag Hand Sannoalc207 Laxxx 1215)
Drug Facts panel for EZ Foam No Alcohol Foaming Instant Hand Sanitizer with Aloe and Vitamin E by Kutol Products Company. It lists benzalkonium chloride 0.13% as the active antibacterial ingredient, usage warnings, directions to apply and rub hands until dry, and inactive ingredients including water, propylene glycol, and aloe. The panel is presented in English, French, and Spanish. Net contents 1000 mL (33.8 Fl. Oz.). Manufactured in USA.*
FDA Label Image

Foaming Instant 1250 mL (68250 1250 Foaming Bag Insthandsan Laxxx 207 1215)

Foaming Instant 1250 mL (68250 1250 Foaming Bag Insthandsan Laxxx 207 1215)
Drug Facts panel for Foaming Instant Hand Sanitizer with Aloe and Vitamin E 1250 mL by Kutol Products Company. It lists the active ingredient benzalkonium chloride 0.13% as an antibacterial agent, with uses for reducing bacteria on skin. The panel includes warnings, directions for use, inactive ingredients, and manufacturer contact details. Text is presented in English, French, and Spanish.*
FDA Label Image

Foaming Instant 950 mL (68278 Clnshape Foaming2015 Ihs 207 1215)

Foaming Instant 950 mL (68278 Clnshape Foaming2015 Ihs 207 1215)
Label for Foaming Instant Hand Sanitizer with Aloe and Vitamin E by Kutol Products Company, Inc. The front label highlights that the product contains no alcohol and offers foaming instant hand sanitizer in a 950 mL (32 Fl. Oz.) size. The back panel includes Drug Facts with the active ingredient Benzalkonium Chloride 0.13%, uses, warnings, directions, and a list of inactive ingredients.*
FDA Label Image

532 mL (68291 Mid Sizepump18oz Laxxxx 207 1215)

532 mL (68291 Mid Sizepump18oz Laxxxx 207 1215)
Foaming Instant Hand Sanitizer with Aloe and Vitamin E by Kutol Products Company, Inc. The label shows an 18 fl oz (532 mL) container of no alcohol hand sanitizer with skin conditioners including aloe and vitamin E. It highlights being non-flammable, non-drying to hands, and easy for soft rub-in. The active ingredient is benzalkonium chloride 0.13% w/w.*
FDA Label Image

Foaming Instant 3.785 L (68209 Foaming Ihs Pour Top Gallon)

Foaming Instant 3.785 L (68209 Foaming Ihs Pour Top Gallon)
Label for Kutol Foaming Instant Hand Sanitizer with Aloe and Vitamin E, a no alcohol hand sanitizer available in a 3.785 liter (one gallon) size. The label highlights the product's antibacterial ingredient benzalkonium chloride 0.13%, usage instructions, warnings, inactive ingredients, and contact information for Kutol Products Company, Inc. in Cincinnati, Ohio. Text appears in English, French, and Spanish.*

* 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.