0.9% Sodium Chloride Injection, Solution
Product Images NDC 51662-1609

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for 0.9% Sodium Chloride (NDC 51662-1609). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, 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

Serialized Label (51662 1609 1 Serialized Rfid Labeling On Bag)

0.9% Sodium Chloride Injection, USP 500 mL intravenous solution in a clear plastic Pleboflex container. The label includes usage instructions, storage conditions, manufacturer information (Grifols, S.A.), and a white barcode sticker indicating it is for demonstration purposes and not for human use. The labeler is HF Acquisition Co LLC, DBA HealthFirst.*

FDA Label Image

Bag (Bag Labeling)

Label for 0.9% Sodium Chloride Injection, USP, 500 mL intravenous solution. The label includes usage, dosage, storage instructions, and manufacturer details. The solution contains 900 mg sodium chloride per 100 mL with specified pH and osmolarity. It notes the container is PVC-free, DEHP-free, and latex-free closure, manufactured by Laboratorios Grifols, S.A., Murcia, Spain under the Grifols brand.*

* 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.