Bnc Hand Sanitizer Antiseptic
Product Images NDC 78419-002

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Bnc Hand Sanitizer Antiseptic (NDC 78419-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bnc Korea 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

Label1 (100 mL)

Label for BNC Hand Sanitizer Antiseptic Gel containing 80% alcohol, labeled as a topical, non-sterile solution with moisturizing formula and Aloe Vera. The label includes Drug Facts with active ingredient alcohol 80% v/v and usage, warnings, directions, inactive ingredients, manufacturer (BNC Korea Co., Ltd.), and volume of 100 mL (3.38 fl. oz.). The design features a green hand icon and a grassy background at the bottom.*

FDA Label Image

Label2 (300 mL)

Label for BNC HAND SANITIZER ANTISEPTIC, a topical solution with 80% alcohol antiseptic. The 300 mL non-sterile solution is indicated to kill 99.9% of germs and contains aloe vera. The label includes detailed Drug Facts with active ingredient, uses, warnings, directions, and other information. Manufactured by BNC Korea Co., Ltd. and made in Korea.*

FDA Label Image

Label3 (500 mL)

The label for BNC HAND SANITIZER ANTISEPTIC displays an 80% alcohol antiseptic topical solution in a 500 mL (16.90 fl. oz.) container. It highlights that it kills 99.9% of germs and contains aloe vera for moisturizing. The label includes drug facts with active ingredient alcohol 80%, usage instructions, warnings, directions, and manufacturer details for BNC KOREA CO., Ltd. It is marked as 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.