Dehydrated Alcohol Injection, Solution
Product Images NDC 51991-999
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Product Visual Gallery
This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Dehydrated Alcohol (NDC 51991-999). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Breckenridge Pharmaceutical 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.
Product Images & Figures Index
Principal Display Panel (5 mL Vial Carton)
This is a description of the product "Dehydrated Alcohol Injection, USP" intended for Cardiac Septal Branch Intra-Arterial Use. The injection contains over 99% ethyl alcohol by volume and is supplied in ten 5 mL single-dose vials. Manufactured by Immacule Lifesciences PV, Ltd in India and distributed by Breckenridge Pharmaceutial, Inc in the USA. Each mL contains 99% ethyl alcohol, and the solution is preservative-free. It is essential to store the product away from any heat source, between 20°C to 25°C, and to avoid refrigeration or freezing. The warning advises against using the injection if discolored or precipitated. The product is highly flammable, and any serious adverse events should be reported to the provided contact number.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.