Sodium Chloride Injection, Solution
Product Images NDC 79672-613

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Sodium Chloride (NDC 79672-613). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nextgen Pharmaceuticals 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

500 mL Container

This is a description of a medical product with the NDC code 79672-613-04. It is a 500mL single dose container of 0.9% Sodium Chloride injection, for intravenous use only. The solution contains 900mg of Sodium Chloride USP and has a pH of 7.0. The container is sterile and should be used according to instructions after squeezing and inspecting the inner bag. The product should be stored at 20-25°C with excursions between 15-30°C, but should be protected from moisture. The packaging contains information about dosage, cautions, and the product itself. The container closure is not made with natural rubber latex.*

FDA Label Image

5000 mL Carton

This is a description of a medical product, specifically a 500mL Fleboflex container containing 0.9% Sodium Chloride Injection USP. The product is manufactured by NEXTGEN and is identified by the code NG 79672-613-40. The product should be stored within the temperature range of 20-25°C, with excursions permissible between 15-30°C. Excessive heat should be avoided. The product is produced by Menwtctrod o N Phamacticas UG and distributed by a company called Brokin located in Y 11207.*

* 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.