Gabgerm Antisec Hand Sanitizer
Product Images NDC 80284-002

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Gabgerm Antisec Hand Sanitizer (NDC 80284-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by International Biotech Factory, S.a. De C.v., 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

1000ml

Gabgerm Antisec hand sanitizer label in blue with white text, showing 33.8 fl oz / 1000 mL volume. The label states it is an antiseptic hand sanitizer that decreases bacteria without water. The active ingredient listed is 72% isopropyl alcohol. Manufacturer information indicates International Biotech Factory, S.A. de C.V. in Mexico, with distributor Mercamericas Inc in Texas. The label includes Drug Facts for use, warnings, directions, inactive ingredients, and a barcode.*

FDA Label Image

Bottle (Bottle)

Gabgerm Antisec hand sanitizer label displaying antiseptic hand sanitizer with 16.9 fl oz (500 mL) volume. The product highlights its germicidal power and germ elimination. The active ingredient is 72% isopropyl alcohol. Manufactured by International Biotech Factory, S.A. de C.V., Mexico. The label includes drug facts, directions, warnings, ingredients, manufacturer details, and a barcode.*

FDA Label Image

Bottle3 (Bottle3)

Gabgerm Antisec hand sanitizer packaging label displays antiseptic hand sanitizer with 72% isopropyl alcohol as the active ingredient. The label highlights its germicidal power and hand bacteria reduction without water. It shows the volume as 8.4 fl oz (250 mL) and includes directions, warnings, ingredients, and manufacturer International Biotech Factory, S.A. de C.V. in Mexico.*

* 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.