Dehydrated Alcohol Injection, Solution
Product Images NDC 50742-539

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Dehydrated Alcohol (NDC 50742-539). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ingenus Pharmaceuticals, 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

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Chemical structure diagram of dehydrated alcohol (ethanol), showing a two-carbon chain with associated hydrogen atoms and a hydroxyl group (OH) at the end.*
FDA Label Image

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FDA Label Image

Dehydrated Alcohol Injection, Usp (Vial Label)

Dehydrated Alcohol Injection, Usp (Vial Label)
The label for Dehydrated Alcohol Injection, USP, 5 mL of ≥99% by volume ethyl alcohol, presented as a single-dose vial. The label specifies use for Cardiac Septal Branch Intra-Arterial administration and indicates discard of unused portions. Manufactured by Ingenus Pharmaceuticals, LLC, made in Germany. Includes storage warnings, a barcode, and space for lot and expiration coding.*
FDA Label Image

Dehydrated Alcohol Injection, Usp -carton Label (149c50c5 59ad 4602 Ad9e 58ad960eb91d 04)

Dehydrated Alcohol Injection, Usp -carton Label (149c50c5 59ad 4602 Ad9e 58ad960eb91d 04)
Packaging label for Dehydrated Alcohol Injection, USP by Ingenus Pharmaceuticals, LLC. The label indicates a 5 mL dosage strength with ≥99% by volume ethyl alcohol. The product is an injection solution for percutaneous use, supplied in boxes containing ten 5 mL single-dose vials. The label highlights storage instructions and warnings about flammability.*

* 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.