Sodium Phosphates Injection, Solution
Product Images NDC 63323-170

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Sodium Phosphates (NDC 63323-170). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, 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

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FDA Label Image

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Label for Sodium Phosphates Injection, USP by Fresenius Kabi USA, LLC. It is a 5 mL single dose vial containing 20 mEq sodium and 15 mmol phosphorus per 5 mL. The label includes dilution instructions, preservative status, and storage conditions with the product NDC 63323-170-05 and lot/expiration number space.*

FDA Label Image

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Sodium Phosphates Injection, USP intravenous solution in single dose vials, each vial 5 mL. Contains 15 mmol phosphorus and 20 mEq sodium per 5 mL. Label indicates 25 vials per package, made by Fresenius Kabi USA, LLC. Label warns that solution must be diluted prior to IV use.*

FDA Label Image

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Label for Sodium Phosphates Injection, USP, 15 mL single dose vial by Fresenius Kabi USA, LLC. It contains 45 mmol phosphorus and 60 mEq sodium per 15 mL. The label states the product must be diluted prior to intravenous use and provides storage instructions and additional product details including preservatives and pH information.*

FDA Label Image

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Label of Sodium Phosphates Injection, USP, 25 x 15 mL single dose vials. Contains 45 mmol phosphorus and 60 mEq sodium per 15 mL. The solution must be diluted prior to intravenous use. Provided by Fresenius Kabi USA, LLC. The label includes storage and handling instructions and indicates the product is preservative free and nonpyrogenic.*

* 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.