Ferric Subsulfate
Product Images NDC 59365-6065

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ferric Subsulfate (NDC 59365-6065). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Coopersurgical, Inc., 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

Astringyn ® Ferric Subsulfate, Aqueous Contents One Dozen (12) 8 Gm Vials Ndc 59365-6065-1 (Astringyn 01)

Astringyn ® Ferric Subsulfate, Aqueous Contents One Dozen (12) 8 Gm Vials Ndc 59365-6065-1 (Astringyn 01)
The image shows the carton label for AstrinGyn Ferric Subsulfate, Aqueous, containing one dozen (12) 8 gram vials. The label includes a caution that Federal (USA) law prohibits dispensing without a prescription. It is labeled by CooperSurgical, Inc., with contact information and the NDC 59365-6065-1 prominently displayed. The label is primarily blue and white with vertical stripe accents.*
FDA Label Image

Principal Display Panel8gm Ndc 59365-6065-0astringyn ®(ferric Subsulfate)aqueous (Astringyn 02)

Principal Display Panel8gm       Ndc 59365-6065-0astringyn ®(ferric Subsulfate)aqueous (Astringyn 02)
Label for ASTRINGYN (Ferric Subsulfate) Aqueous by CooperSurgical, Inc. The product contains Ferric Subsulfate 259 mg/g with 0.0638 mg of Fe3+ per ml, preserved with benzalkonium chloride 0.005%, povidone USP 23.2%, glycerin USP 13.3%, and purified water. It is an 8 gm single-use dose vial, with storage instructions to keep at controlled room temperature 15-30°C and to discard after use. The label also includes reference number 6065 and NDC 59365-6065-0.*

* 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.