Turkfleks %0.9 Sodium Chloride
Product Images NDC 85160-200

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 Turkfleks %0.9 Sodium Chloride (NDC 85160-200). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Turk Ilac Ve Serum Sanayi Anonim Sirketi, 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

Fda Approved (Fda Approved)

Fda Approved (Fda Approved)
Packaging labels of 0.9% Sodium Chloride Injection USP intravenous bags in 1000 ml, 500 ml, 250 ml, and 100 ml sizes. Each bag is clear and labeled with concentration and volume information. The bags are from the manufacturer Baxter, displaying typical medical infusion bag features including ports and hang-tabs.*
FDA Label Image

Turkfleks (Label Turkfleks)

Turkfleks (Label Turkfleks)
Turkfleks %0.9 Sodium Chloride intravenous infusion solution in a 500 mL bag. The label shows isotonic sodium chloride concentration, composition details per 100 mL, usage instructions, and manufacturer information from TURK ILAC VE SERUM SANAYI ANONIM SIRKETI, including contact details and packaging symbols. Text is primarily in Turkish.*
FDA Label Image

Package Label.principal Display Panel (Package Label.principal Display Panel)

Package Label.principal Display Panel (Package Label.principal Display Panel)
Turkfleks %0.9 Sodium Chloride solution in a 500 mL flexible IV bag for infusion. The label includes usage instructions, storage conditions, and administration guidance in Turkish. The labeler is TURK ILAC VE SERUM SANAYI ANONIM SIRKETI.*

* 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.