Dr. Daddys Hand Sanitizer
Product Images NDC 76884-0001

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Dr. Daddys Hand Sanitizer (NDC 76884-0001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Tb Healthcare Co., Ltd., 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

2 (Drugfacts 500ml)

Drug Facts panel for Dr. Daddys Hand Sanitizer, volume 16.9 fl. oz. / 500 ml. Lists active ingredient as 70% alcohol for antiseptic use. Includes uses to reduce bacteria when soap and water are unavailable, warnings about flammability and avoiding use on young children or wounds, directions for proper application, storage instructions, and a list of inactive ingredients. Contact information for questions or comments is provided.*

FDA Label Image

1 (Label 500)

Dr. Daddys Hand Sanitizer packaging label displays the product name and identifies it as a hand sanitizer with 70% ethanol, claiming to kill 99.9% of germs. The label lists ingredients including ethanol, green tea extract, aloe, and chamomile. It provides usage instructions, precautions, storage information, manufacturer K.Boeun Pharmaceutical Co., Ltd., seller TB Healthcare Co., Ltd., and a 500 ml volume. The label includes a barcode and recycling symbols and notes the product is made in Korea.*

* 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.