Antibacterial Hand Sanitizer
Product Images NDC 78634-002

8 FDA label images from Dongguan Boze Technology Co., Ltd · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Antibacterial Hand Sanitizer (NDC 78634-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dongguan Boze Technology 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

1 (1)

1 (1)
Drug Facts label of ANTIBACTERIAL HAND SANITIZER SPRAY by Dongguan Boze Technology Co., LTD. Lists Ethyl Alcohol 75% W/W as the active ingredient with antiseptic purpose. Provides uses, warnings, directions, inactive ingredients, manufacturer and distributor details, plus safety and usage instructions.*
FDA Label Image

2 (2)

2 (2)
Drug Facts panel for ANTIBACTERIAL HAND SANITIZER SPRAY with active ingredient Ethyl Alcohol 75% W/W as antiseptic. It lists uses for decreasing bacteria on skin and recommends repeat use. Includes warnings for external use, flammability, and avoiding eye and nose contact. Directions state to place a small amount on hands and rub until dry. Contains a list of inactive ingredients and manufacturer and distributor information.*
FDA Label Image

3 (3)

3 (3)
Text panel from the ANTIBACTERIAL HAND SANITIZER SPRAY by Dongguan Boze Technology Co., Ltd. It lists Ethyl Alcohol 75% W/W as the active ingredient and antiseptic. The panel includes usage instructions, warnings about flammability and eye contact, directions for use, inactive ingredients, and manufacturing and distribution details.*
FDA Label Image

4 (4)

4 (4)
Drug Facts panel for ANTIBACTERIAL HAND SANITIZER SPRAY containing 75% Ethyl Alcohol as the active ingredient. The panel includes purpose, usage warnings, directions, inactive ingredients, manufacturer and distributor information, and safety precautions such as keeping away from heat and flame, avoiding eye and nose contact, and supervision advice for children under 6 years.*
FDA Label Image

5 (5)

5 (5)
Drug Facts panel for ANTIBACTERIAL HAND SANITIZER SPRAY listing ethyl alcohol 75% w/w as the active ingredient and antiseptic purpose. Includes uses for hand sanitizing to decrease bacteria, warnings for external use and flammability, directions for application, inactive ingredients, and manufacturer information for Dongguan Boze Technology Co., LTD.*
FDA Label Image

6 (6)

6 (6)
Drug Facts panel for ANTIBACTERIAL HAND SANITIZER SPRAY showing Ethyl Alcohol 75% w/w as the active ingredient with antiseptic purpose. Includes uses, warnings about external use and flammability, directions for use, inactive ingredients, and manufacturer and distributor information. Safety advice for children and contact with eyes is also presented.*
FDA Label Image

7 (7)

7 (7)
Drug Facts panel for Antibacterial Hand Sanitizer Spray by Dongguan Boze Technology Co., LTD. It lists Ethyl Alcohol 75% w/w as the active ingredient for antiseptic use, along with precautions, directions for use, and inactive ingredients including water and propanediol. The label includes warnings about external use, flammability, and supervision for children under 6, plus manufacturer and distributor information.*
FDA Label Image

8 (8)

8 (8)
Drug Facts panel for ANTIBACTERIAL HAND SANITIZER SPRAY showing the active ingredient as Ethyl Alcohol 75% w/w with antiseptic purpose. It includes usage warnings, directions for use, and inactive ingredients such as water, propanediol, polyacrylic acid, triethylamine, and glycerin. The product is manufactured by Dongguan Boze Technology Co., LTD and distributed by Elegant Headwear Co., Inc.*

* 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.