Katra Hand Sanitizer
Product Images NDC 81103-002

3 FDA label images from Ths Cosmetic Eood · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Katra Hand Sanitizer (NDC 81103-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ths Cosmetic Eood, 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

Image (8110300210)

Image (8110300210)
KATRA Hand Sanitizer spray with 75% ethyl alcohol, containing chamomile extract. The label shows 1000 ml (33.81 fl oz) bottle size. The product is marketed by THS COSMETIC EOOD, highlighting antiseptic use with no rinsing required. The label includes Drug Facts with active ingredient, usage directions, warnings, inactive ingredients, and storage instructions.*
FDA Label Image

Image (8110300224)

Image (8110300224)
Label for KATRA Hand Sanitizer spray, 8.12 fl. oz (240 ml), containing 75% ethanol (ethyl alcohol) as active antiseptic ingredient. The label highlights chamomile extract and no rinsing required. Distributed by V&G Commerce LLC, made in the European Union. Includes drug facts, warnings, directions, inactive ingredients, and storage information.*
FDA Label Image

Image (8110300250)

Image (8110300250)
The image shows the label of KATRA Hand Sanitizer spray refill, 5.0 L (169 fl. oz., 10.57 pt) with 75% ethyl alcohol as the active ingredient. It features chamomile extract, is made in the European Union, and is distributed by V&G Commerce LLC. The label includes drug facts with usage, warnings, directions, and inactive ingredients.*

* 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.