Sodium Acetate Anhydrous Solution, Concentrate
Product Images NDC 70069-047

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 Sodium Acetate Anhydrous (NDC 70069-047). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Somerset Therapeutics, 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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Sodium Acetate Injection USP 100 mEq/50 mL (2 mEq/mL) intravenous solution concentrate label. Pharmacy bulk package, 50 mL vial. Manufactured for Somerset Therapeutics, LLC, Somerset, NJ. Contains sodium acetate anhydrous 164 mg/mL. Label includes storage instructions, dilution caution, and usage directions. Made in India.*
FDA Label Image

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Label for Sodium Acetate Injection, USP 100 mEq/50 mL (2 mEq/mL) solution concentrate for intravenous use. The packaging is a pharmacy bulk package of 25 vials, each 50 mL, manufactured by Somerset Therapeutics, LLC. The label includes storage instructions and a caution that the product must be diluted before use.*
FDA Label Image

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Label for Sodium Acetate Injection, USP 200 mEq/100 mL (2 mEq/mL) solution concentrate for intravenous use. The label includes warnings that this is a pharmacy bulk package not for direct infusion and must be diluted. It is manufactured for Somerset Therapeutics, LLC, made in India, and contains scale and usage instructions.*
FDA Label Image

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Sodium Acetate Injection, USP 200 mEq/100 mL (2 mEq/mL) solution concentrate for intravenous use, packaged by Somerset Therapeutics LLC. The label states caution for dilution, pharmacy bulk package, not for direct infusion, and specifies sterility and storage conditions. The packaging is designed for 20 x 100 mL vials with an NDC of 70069-048-20.*

* 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.