Zinc Sulfate Solution
Product Images NDC 70069-691

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Zinc Sulfate (NDC 70069-691). 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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Chemical structure diagram of zinc sulfate showing a central zinc ion bonded to sulfate groups and surrounding water molecules, illustrating the compound's hydrated form.*
FDA Label Image

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Label for Zinc Sulfate Injection, USP 25 mg per 5 mL (5 mg/mL) solution for intravenous use. The product is a sterile pharmacy bulk package not for direct infusion, requiring dilution and admixing before intravenous administration. Manufactured for Somerset Therapeutics, LLC, Somerset, NJ, and made in India. Storage and dosage instructions are partially visible.*
FDA Label Image

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Carton label for Zinc Sulfate Injection, USP 25 mg/5 mL (5 mg/mL) solution for intravenous use, manufactured by Somerset Therapeutics, LLC. The label indicates a pharmacy bulk package containing 25 vials of 5 mL each, with instructions that it is not for direct infusion but for use after dilution and admixing.*
FDA Label Image

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Label for Zinc Sulfate Injection, USP solution, 30 mg/10 mL (3 mg/mL) sterile intravenous solution. The label indicates it is a pharmacy bulk package not for direct infusion, manufactured by Somerset Therapeutics, LLC. The product is made in India and includes storage, usage, and contact details.*
FDA Label Image

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Zinc Sulfate Injection, USP 30 mg per 10 mL (3 mg/mL) solution for intravenous use in a pharmacy bulk package with 25 vials of 10 mL each. The label includes storage instructions, manufacturer Somerset Therapeutics, LLC, and states it is sterile and not for direct infusion, requiring dilution and admixing prior to intravenous 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.