Hand Sanitizer
Product Images NDC 74077-1157

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 74077-1157). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Faber Sanitizer, 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

Inactive Ingredients (Faber Sanitizer Inactive Ingredients)

Label for Hand Sanitizer by Faber Sanitizer shows 1 liter (33.8 oz) volume and is produced by Faber Distilling Co. It states 'DO NOT DRINK! For external use only, use only on hands.' Active ingredient is 80% ethanol as an antiseptic. The label includes warnings, directions for use, and contact information, with a recommended formulation by the World Health Organization.*

FDA Label Image

Indications And Uses (Faber Sanitizer Indications And Uses)

Label for Hand Sanitizer by Faber Sanitizer showing 1 liter (33.8 oz) volume. The label includes warnings such as "Do Not Drink!" and states it is for external use only. Active ingredient is 80% ethanol as an antiseptic. The label also provides directions, storage information, and a barcode. Recommended formulation by World Health Organization.*

FDA Label Image

Otc Active Ingredients (Faber Sanitizer Otc Active Ingredients)

Label for Faber Sanitizer Hand Sanitizer, a topical solution containing 80% ethanol as an antiseptic active ingredient. The label indicates a 1-liter (33.8 oz) container produced by Faber Distilling Co. It includes warnings about external use only, flammability, and instructions for use. The formulation is recommended by the World Health Organization.*

FDA Label Image

Otc Keep Out Of Reach Of Children (Faber Sanitizer Out Of Reach Of Children)

Label for Hand Sanitizer by Faber Sanitizer, containing 1 liter (33.8 oz). The label highlights the product as an alcohol antiseptic with 80% ethanol, intended for external use only on hands. It includes warnings, directions for use, and ingredients, with a prominent notice 'DO NOT DRINK!' and notes the formulation is recommended by the World Health Organization.*

FDA Label Image

Otc Purpose (Faber Sanitizer Purpose)

Label of Hand Sanitizer by Faber Sanitizer, containing 1 liter (33.8 oz). The label states it is produced by Faber Distilling Co. with an active ingredient of 80% ethanol as an antiseptic. It includes warnings, directions, inactive ingredients, and storage information, and advises for external use only. The label features a barcode and notes it is made in Pennsylvania.*

FDA Label Image

Warnings (Faber Sanitizer Warnings)

Label for Hand Sanitizer by Faber Sanitizer showing 1L (33.8 oz.) volume. Features active ingredient Ethanol 80% as antiseptic. Label includes warnings, directions, inactive ingredients, and states it is made in PA by Faber Distilling Co. Large "DO NOT DRINK!" warning and usage instructions for external use only are also prominent.*

FDA Label Image

Package Label (Package Label)

Packaging label for Faber Sanitizer Hand Sanitizer featuring 1 liter (33.8 oz) volume. The label highlights 80% ethanol as the active ingredient and includes drug facts, warnings, and directions for use. It is marked as made in Pennsylvania and displays a barcode at the bottom right.*

FDA Label Image

Doesage And Administration (Doseage And Administration)

Label for Hand Sanitizer by Faber Sanitizer. The label indicates an alcohol antiseptic topical solution with 80% ethanol as the active ingredient. It specifies a 1L (33.8 oz) volume and includes warnings such as flammability and external use only. The product is made in Pennsylvania by Faber Distilling Co. and uses a formulation recommended by the World Health Organization.*

* 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.