Hand Sanitizer
Product Images NDC 75791-505

7 FDA label images from Aurum Sierra Inc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 75791-505). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurum Sierra 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

1 Gal Label (Ddd 1 Hand Sanitizer Label)

1 Gal Label (Ddd 1 Hand Sanitizer Label)
Packaging label for Hand Sanitizer by Dry Diggings Distillery, containing 80% alcohol antiseptic in a non-sterile topical solution form. The bottle size is 3785 mL (1 gallon). The label includes the NDC number 75791-505-07 and the product is associated with Aurum Sierra Inc.*
FDA Label Image

10 Oz Label (Ddd 10 Oz Hand Sanitizer Label)

10 Oz Label (Ddd 10 Oz Hand Sanitizer Label)
Hand Sanitizer front and back labels by Aurum Sierra Inc under the Dry Diggings Distillery brand. The front label states 80% alcohol antiseptic topical solution, non-sterile, 296 mL (10 oz) with NDC 75791-505-06. The back label includes Drug Facts with active ingredient alcohol 80%, uses, warnings, directions, other information on storage, and inactive ingredients glycerin, hydrogen peroxide, purified water USP.*
FDA Label Image

12 Oz Label (Ddd 12oz Hand Sanitizer Label)

12 Oz Label (Ddd 12oz Hand Sanitizer Label)
Label for Hand Sanitizer by Dry Diggings Distillery showing the product as an 80% alcohol antiseptic topical and non-sterile solution in a 355 mL (12 oz) bottle. The label includes the NDC number 75791-505-01. A drug facts panel listing active ingredient, uses, warnings, directions, and inactive ingredients is partially visible.*
FDA Label Image

2.5 Gal Label (Ddd 2.5 Hand Sanitizer Label)

2.5 Gal Label (Ddd 2.5 Hand Sanitizer Label)
The image shows the front and back label of Dry Diggings Distillery Hand Sanitizer. The front label indicates it is an 80% alcohol antiseptic topical, non-sterile solution in a 9464 mL (2.5 gallon) container with NDC 75791-505-02. The back label presents detailed Drug Facts including active ingredient, uses, warnings, directions, storage instructions, and inactive ingredients such as glycerin, hydrogen peroxide, and purified water USP.*
FDA Label Image

270 Gal Label (Ddd 270 Hand Sanitizer Label)

270 Gal Label (Ddd 270 Hand Sanitizer Label)
Label for Hand Sanitizer by Aurum Sierra Inc, showing the product name 'Dry Diggings Distillery Hand Sanitizer' with 80% alcohol antiseptic as the active ingredient. The label specifies it as a non-sterile topical solution with a volume of 1021950 mL (270 gallons). The NDC number 75791-505-04 is also visible.*
FDA Label Image

55 Gal Label (Ddd 55 Hand Sanitizer Label)

55 Gal Label (Ddd 55 Hand Sanitizer Label)
This image shows the front label of a hand sanitizer product named Dry Diggings Distillery Hand Sanitizer containing 80% alcohol antiseptic as the active ingredient. It is a non-sterile topical solution packaged in a large container with a volume of 208198 mL (55 gallons). The label includes the NDC number 75791-505-03 and the product is labeled by Aurum Sierra Inc.*
FDA Label Image

8 Oz Label (Ddd 8 Oz Hand Sanitizer Label)

8 Oz Label (Ddd 8 Oz Hand Sanitizer Label)
The image shows the front and back labels of Hand Sanitizer by Aurum Sierra Inc, NDC 75791-505-05. The front label identifies the product as a non-sterile topical alcohol antiseptic solution with 80% alcohol, volume 237 mL (8 oz). The back label includes Drug Facts listing active ingredient, uses, warnings, directions, other information, and inactive ingredients.*

* 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.