Aquasol A Parenteral Injection, Solution
Product Images NDC 64980-721

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Aquasol A Parenteral (NDC 64980-721). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rising Pharma Holdings, 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

Aquasol-carton-label (Aquasol Carton Label)

This text appears to contain information about a pharmaceutical product, specifically a form of vitamin A called Retinyl Palmitate. It provides details such as its concentration (50,000 USP units/15 mg) and instructions for use (intramuscular administration). The product is described as sterile and packaged in single-dose vials. There are also indications regarding storage conditions (2°C to 8°C) and a caution not to freeze the product. Additionally, the text includes details about the manufacturer and distributor of the product.*

FDA Label Image

Aquasol-struc (Aquasol Struc)

FDA Label Image

Aquasol-vial-label.jpg (Aquasol Vial Label)

This text describes a pharmaceutical product with NDC number 64980-721-02, distributed by Rising Pharma Holdings, Inc. The product is a 50,000 USP units/mL Water-Miscible Retinyl Palmitate solution, containing 15 mg of retinol, intended for Intramuscular Use. It comes in a 2mL Single-Dose Vial. The product is made in India and has a manufacturer code TN/DRUGS/616/1996. It was issued on 01/2026.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.