Sodium Edecrin
Product Images NDC 25010-210

4 FDA label images from Bausch Health Us, Llc · 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 Sodium Edecrin (NDC 25010-210). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bausch Health Us, 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

Chemical Structure (Edecrin 01)

Chemical Structure (Edecrin 01)
Chemical structure of the active ingredient in SODIUM EDECRIN 25 mg, shown as a molecular diagram with chlorine atoms, carboxyl, and ketone functional groups. The structure represents the compound's arrangement of atoms and bonds.*
FDA Label Image

Chemical Structure (Edecrin 02)

Chemical Structure (Edecrin 02)
Chemical structure of the active ingredient in SODIUM EDECRIN 25 mg, showing a chlorinated aromatic ring with attached methoxycarboxylate and keto-ethyl side groups.*
FDA Label Image

Image 01

Image 01
Label for Edecrin (Ethacrynic Acid) 25 mg tablets by Bausch Health US, LLC. The label includes the NDC 25010-215-15, indicates a quantity of 100 tablets, and specifies storage instructions. The product trademark and manufacturer details for Bausch Health Companies Inc., Canada, are also shown.*
FDA Label Image

Image 02

Image 02
Packaging label for SODIUM EDECRIN 50 mg/vial intravenous injection, containing ethacrynate sodium equivalent to 50 mg ethacrynic acid. The label shows it is a single-dose vial supplied by Bausch Health US, LLC, with storage and usage instructions including reconstitution details and dosage information.*

* 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.