Aminocaproic Acid Injection, Solution
Product Images NDC 0404-9812

3 FDA label images from Henry Schein, Inc. · 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 Aminocaproic Acid (NDC 0404-9812). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Henry Schein, 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

FDA Label Image

Image1.jpg (Image1)

Image1.jpg (Image1)
A table showing the unit of sale and concentration for aminocaproic acid injection. The unit of sale is a tray containing 25 single-dose fliptop vials, each vial holding 20 mL in a 30 mL container, with an NDC of 0409-4346-73. The concentration is 5 grams per 20 mL, equivalent to 250 mg/mL.*
FDA Label Image

Image2.jpg (Image2)

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A text panel referencing a publication: Stefanini, M. and Dameshek, W., The Hemorrhagic Disorder, Ed. 2, New York, Grune and Stratton, pp. 510-514, 1962. Also includes the Hospira logo, distributor information (Hospira, Inc., Lake Forest, IL 60045 USA), a label number (LAB-0948-3.0), and a revision date of 6/2018.*
FDA Label Image

Label1.jpg (Label1)

Label1.jpg (Label1)
Label for Aminocaproic Acid injection, USP, 5 g/20 mL (250 mg/mL) single-dose vial. Instructions note that the solution must be diluted for intravenous use, sterile, nonpyrogenic, and contain no bacteriostat. The label includes storage instructions, lot number, expiration date, NDC 0404-9812-20, and packaging information indicating Henry Schein, Inc. as the labeler at Bastian, VA.*

* 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.