Generic -hand Sanitizer
Product Images NDC 78985-001

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Generic -hand Sanitizer (NDC 78985-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Generic Specialties, Inc., 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

Observationmedia (1000ml)

Label for Generic -Hand Sanitizer by Generic Specialties, Inc., showing a 33.8 FL OZ (1000 ml) bottle. The label highlights 2X sanitizing strength, moisturizing formula with vitamin E, and describes it as a refreshing gel. Active ingredient is ethyl alcohol 70% v/v. Included are Drug Facts, warnings, directions, and storage information, along with a barcode and expiration date of 01/2022.*

FDA Label Image

Observationmedia (100ml)

The image shows the front and back label of Generic -Hand Sanitizer distributed by Generic Specialties, Inc. The front label highlights '2X Sanitizing Strength' and states the product is a moisturizing hand sanitizer gel with vitamin E, providing 3.38 FL OZ (100 ml). The back label includes Drug Facts with Ethyl alcohol 70% v/v as the active ingredient, uses, warnings, directions, and storage information.*

FDA Label Image

Observationmedia (200ml)

Packaging label for Generic -Hand Sanitizer by Generic Specialties, Inc. The label indicates a 6.76 FL OZ (200 ml) bottle of moisturizing hand sanitizer gel with 2x sanitizing strength and vitamin E. The active ingredient is ethyl alcohol 70% v/v. The product is described as a non-sterile solution that kills 99.9% of illness-causing germs and leaves hands feeling soft.*

FDA Label Image

Observationmedia (350ml)

Label of Generic -Hand Sanitizer moisturizing refreshing gel in an 11.83 FL OZ (350 ml) bottle. The front highlights 2X sanitizing strength, non-sterile solution, kills 99.9% of illness-causing germs, and contains vitamin E. The back displays drug facts including active ingredient ethyl alcohol 70% v/v, warnings, directions, and inactive ingredients. Distributed by Generic Specialties, Inc.*

FDA Label Image

Observationmedia (5000ml)

Packaging label of Generic Hand Sanitizer moisturizing non-sterile gel with Vitamin E, 169 fl oz (5000 ml) from Generic Specialties, Inc. The front highlights 2X sanitizing strength and killing 99.9% of illness-causing germs. The back includes drug facts with active ingredient ethyl alcohol 70% v/v and usage warnings.*

FDA Label Image

Observationmedia (500ml)

Generic Hand Sanitizer 16.9 FL OZ (500 ml) moisturizing gel with vitamin E in a non-sterile solution. Label highlights 2X sanitizing strength and claims to kill 99.9% of illness-causing germs. Distributed by Generic Specialties, Inc. The active ingredient is ethyl alcohol 70% v/v.*

FDA Label Image

Observationmedia (50ml)

Label of Generic -Hand Sanitizer moisturizing gel, 1.69 fl oz (50 ml), by Generic Specialties, Inc. The front displays the product name with claims of 2x sanitizing strength, kills 99.9% of illness-causing germs, contains vitamin E, and is a non-sterile solution. The back includes Drug Facts with active ingredient ethyl alcohol 70% v/v, usage directions, warnings, inactive ingredients, storage instructions, and distributor contact information.*

FDA Label Image

Observationmedia (89ml)

Generic Hand Sanitizer moisturizing non-sterile solution travel size 3 fl oz (89 ml) bottle label by Generic Specialties, Inc. Front highlights 2X sanitizing strength, kills 99.9% of illness-causing germs, contains vitamin E, and is a refreshing gel. The back panel shows drug facts including active ingredient ethyl alcohol 70% v/v and usage directions and warnings.*

* 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.