Hand Sanitizer
Product Images NDC 75133-101

3 FDA label images from Black Draft Farm Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 75133-101). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Black Draft Farm Llc, 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

64oz Comp

64oz Comp
Hand Sanitizer topical solution in two white plastic gallon jugs with handles and white screw caps. The label indicates 80% alcohol antiseptic strength, 64 fluid ounces (1.89L) volume, and describes it as a non-sterile solution. The label includes usage instructions, warnings, ingredients, and the product is labeled by Black Draft Farm LLC.*
FDA Label Image

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A2fa3ef2 D363 499e E053 2995a90abab5 (2)
Hand Sanitizer topical solution 80% alcohol antiseptic, non-sterile, in a 120 mL (4 fl oz) white plastic bottle with a white cap. The front label displays the product name and key ingredient concentration. The back label contains drug facts including active ingredient, warnings, directions, and manufacturer information for Black Draft Farm LLC in Martinsburg, West Virginia.*
FDA Label Image

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B6864e87 38cb D5d6 E053 2a95a90a6881
Hand Sanitizer alcohol antiseptic 80% topical solution in a 120 mL (4 fl oz) white plastic bottle. The front label states 'Hand Sanitizer non-sterile solution' with an illustration of two hands clasped. The rear label includes Drug Facts, usage directions, warnings, ingredients, and the producer Black Draft Distillery located in Martinsburg, West Virginia.*

* 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.