Hand Sanitizer
Product Images NDC 75477-435

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 75477-435). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Transliquid Technologies, Llc, 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

250ml Back.

Drug Facts panel for Hand Sanitizer 8oz by Transliquid Technologies, LLC. It lists ethyl alcohol 70% as the active ingredient with antiseptic purpose, usage information, warnings for external use and flammability, directions for use, inactive ingredients including glycerin and triethanolamine, storage conditions, and manufacturer details. Contact information and expiration timeframe are also included.*

FDA Label Image

250ml Front

Label for Mystic Shield Protection Hand Sanitizer 8oz, alcohol antiseptic 70% topical solution. The label highlights it as an antiseptic hand rub, non-sterile solution, with extra strength formula, and claims to kill harmful bacteria and germs. The volume stated is 8.45 fl. oz. (250 ml).*

FDA Label Image

500mlback

The image shows a Drug Facts panel for Hand Sanitizer 8oz by Transliquid Technologies, LLC. It lists ethyl alcohol 70% v/v as the active antiseptic ingredient, usage instructions, warnings about flammability and age restrictions, directions for use, storage information, and a contact number for questions or comments. The batch number is printed separately on the container.*

FDA Label Image

500mlfront

Label for Mystic Shield Protection Alcohol Antiseptic 70% Topical Solution, an antiseptic hand rub non-sterile solution. The label highlights an extra strength formula claiming to kill harmful bacteria and germs. The volume indicated is 16.9 fl. oz. (500 ml).*

FDA Label Image

Back 120ml

Drug Facts panel for Hand Sanitizer 8oz showing active ingredient Ethyl Alcohol 70% v/v as antiseptic. Details include antiseptic purpose, usage instructions to reduce bacteria, warnings for external use only and flammability, directions for application, storage instructions to store between 15-50°C and avoid freezing, and inactive ingredients such as glycerin and purified water. Manufacturer is Mytic Intl S.A. de C.V.*

FDA Label Image

Front 120ml

Label of Hand Sanitizer 8oz by Transliquid Technologies, LLC featuring Mystic Shield Protection branding. The label states it is an alcohol antiseptic topical solution with 70% alcohol content. It is described as an antiseptic hand rub, non-sterile solution with an extra strength formula and claims to kill harmful bacteria and germs. The bottle size is 4.05 fl. oz. (120 ml).*

FDA Label Image

Sachet Back

Drug Facts panel for Hand Sanitizer 8oz by Transliquid Technologies, LLC. Lists ethyl alcohol 70% as active ingredient, indicates antiseptic use, usage instructions, warnings, storage conditions, inactive ingredients, contact info, and expiration details.*

FDA Label Image

Sachet Front

Label for Off U Go Hand Sanitizer containing 70% alcohol antiseptic. The label claims it kills 99.9% of bacteria. The volume noted is 0.07 fl. oz. / 2 ml. The product is associated with Transliquid Technologies, LLC.*

FDA Label Image

Etiquetatote

Label for Hand Sanitizer 8oz by Transliquid Technologies, LLC featuring the product name in bold with the company logo at the top. The label includes Drug Facts with ethyl alcohol 70% as the active ingredient and lists warnings, directions, storage information, and inactive ingredients. Hazard symbols for flammability and caution are present, along with a barcode and distribution details.*

* 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.