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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.
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Dehydrated Alcohol Injection, Usp (Vial Label)
Description: This text provides information regarding a dehydrated alcohol injection solution, advising caution against use if discolored or precipitated. It also includes storage instructions, dosage guidelines for cardiac septal branch use, and details about the manufacturer, Ingenus Pharmaceuticals, LLC. The product is identified by LOT and NDC numbers.*
Dehydrated Alcohol Injection, Usp -carton Label (149c50c5 59ad 4602 Ad9e 58ad960eb91d 04)
This text appears to be a description of a Dehydrated Alcohol Injection, USP. It mentions the sterile, preservative-free solution containing 5 mL of 299% by volume ethyl alcohol for Cardiac Septal Branch. The solution comes in ten 5 mL single-dose vials, and any unused portion should be discarded. It also warns that the solution is highly flammable and for external use only.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
