Chromacleanse Hand Sanitizer
Product Images NDC 74172-112

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Chromacleanse Hand Sanitizer (NDC 74172-112). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Chromaflo Technologies Corp, 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

Back Panel (Chromaflo Sanitizer Ethyl Acohol Back Panel 16 Oz. Bottle)

Back Panel (Chromaflo   Sanitizer   Ethyl Acohol   Back Panel   16 Oz. Bottle)
This is a Drug Facts label for a hand sanitizer product containing 80% ethyl alcohol. It is intended to be used to reduce bacteria that can cause disease when soap and water are not available. The product is only to be used externally and should be kept away from heat or flame. Children under two months of age should not use this product, and it should not be used on open skin wounds. If the product comes in contact with eyes, rinse eyes thoroughly with water. If irritation or rash occurs, stop using the product and consult a doctor. The hand sanitizer should be applied to cover all surfaces of the hands and should be rubbed until dry. Children under six years old should be supervised when using the product to avoid swallowing it. The product should be stored between 15-30°C and should be protected from freezing and excessive heat. The inactive ingredients are glycerin, hydrogen peroxide, and purified water USP.*
FDA Label Image

Front Panel (Chromaflo Sanitizer Ethyl Acohol Front Panel 16 Oz. Bottle)

Front Panel (Chromaflo   Sanitizer   Ethyl Acohol   Front Panel   16 Oz. Bottle)
ChromaCleanse™ is a hand sanitizer with 80% antiseptic Ethyl Alcohol as its active ingredient. It comes in a non-sterile topical solution of 473 mL and is manufactured by Chromaflo Technologies Corp. in Ashtabula, GH 44004. This formula is recommended by FD4.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.