Atropine Sulfate Solution/ Drops
Product Images NDC 70069-716

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Atropine Sulfate (NDC 70069-716). 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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Image (07ece291 B401 4c28 9c81 6b686aa36e07 01)
Chemical structure of Atropine Sulfate Monohydrate showing the molecular arrangement including the tropane ring system, ester functional group linked to a phenyl ring, and associated sulfate and water molecules.*
FDA Label Image

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Image (07ece291 B401 4c28 9c81 6b686aa36e07 02)
Label for Atropine Sulfate Ophthalmic Solution USP 1% in a 5 mL sterile solution form. The label includes the active ingredient atropine sulfate monohydrate 1%, preservative benzalkonium chloride 0.01%, and inactive ingredients, along with storage instructions and manufacturing details by Somerset Therapeutics, LLC. The product is for eye use only and is Rx only.*
FDA Label Image

Image (07ece291 B401 4c28 9c81 6b686aa36e07 03)

Image (07ece291 B401 4c28 9c81 6b686aa36e07 03)
Label for Atropine Sulfate Ophthalmic Solution USP 1%, a sterile eye drop solution in a 5 mL bottle. The label includes the National Drug Code (NDC) 70069-716-01, lists active ingredient atropine sulfate monohydrate 1%, and shows preservatives and inactive ingredients. Manufactured for Somerset Therapeutics, LLC, the label features directions for storage and a customer care contact number.*

* 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.