Ammonul
Product Images NDC 62592-720

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 Ammonul (NDC 62592-720). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ucyclyd Pharma 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.

FDA Label Image

Chemical Structure (Ammonul 01)

Chemical Structure (Ammonul 01)
Chemical structure diagram showing sodium phenylacetate and sodium benzoate, two active ingredients associated with the product Ammonul by Ucyclyd Pharma Inc.*
FDA Label Image

Figure 2 (Ammonul 02)

Figure 2 (Ammonul 02)
An illustration depicting the urea cycle and nitrogen disposal pathway. It shows the biochemical steps involving amino acids and intermediates such as ornithine, citrulline, argininosuccinate, and arginine. Enzymes like CPS, OTC, ASS, ASL, and ARG are labeled, as well as the conversion of benzoate to hippurate and phenylacetate to phenylacetylglutamine for urine excretion. The diagram highlights how nitrogen is processed and eliminated.*
FDA Label Image

Principal Display Panel (50 mL Vial Carton)

Principal Display Panel (50 mL Vial Carton)
Ammonul 10%/10% injection label shows it contains sodium phenylacetate and sodium benzoate. The 50 mL vial is for intravenous use only and requires dilution before administration. The label includes dosage information and manufacturer Ucyclyd Pharma Inc. along with an NDC barcode and warnings for use.*
FDA Label Image

Principal Display Panel (50 mL Vial Carton)

Principal Display Panel (50 mL Vial Carton)
The image shows the packaging label for Ammonul injection by Ucyclyd Pharma Inc. It is a 50 mL vial with a 10% sodium phenylacetate and 10% sodium benzoate composition. The label includes storage instructions, usage warning, and manufacturing details, indicating it is for IV use only and must be diluted before administration.*

* 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.