Atropine Sulfate Solution/ Drops
Product Images NDC 70069-582

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Atropine Sulfate (NDC 70069-582). 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 of atropine sulfate showing its molecular composition including a tropane ring, ester linkage, and benzene ring, along with associated sulfate and water molecules.*

FDA Label Image

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Label for Atropine Sulfate Ophthalmic Solution 1%, 2 mL. The label lists active ingredient Atropine sulfate 10 mg/mL and preservative Benzalkonium Chloride 0.1 mg/mL. It indicates the product is sterile and for topical eye use. Storage instructions specify 20° to 25°C and to keep the container tightly closed. Manufactured for Somerset Therapeutics, LLC, made in India, includes NDC 70069-581-01.*

FDA Label Image

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Label for Atropine Sulfate Ophthalmic Solution, USP 1%, 2 mL sterile drops by Somerset Therapeutics LLC. The label includes NDC 70069-581-01, directions for topical eye application, active ingredient at 10 mg/mL, and a list of inactive ingredients. Storage instructions and safety warnings are present along with company contact information.*

FDA Label Image

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Label for Atropine Sulfate Ophthalmic Solution USP 1%, a sterile eye drop solution. Each mL contains 10 mg atropine sulfate with 0.1 mg preservative benzalkonium chloride. The label indicates 5 mL volume, storage instructions at 20° to 25°C, and manufacturer Somerset Therapeutics, LLC, Somerset, NJ, with the product made in India.*

FDA Label Image

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Packaging label for Atropine Sulfate Ophthalmic Solution USP 1%, 5 mL sterile eye drops by Somerset Therapeutics LLC. The label includes usage instructions, storage conditions (20° to 25°C), inactive ingredients, and a warning to keep out of reach of children. The product is made in India and intended for topical application to the eye.*

* 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.