0.9% Sodium Chloride Injection, Solution
Product Images NDC 51662-1577

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for 0.9% Sodium Chloride (NDC 51662-1577). 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.

Product Images & Figures Index

FDA Label Image

Bag (Bag Labeling)

Bag (Bag Labeling)
Label for 0.9% Sodium Chloride Injection, USP, 500 mL intravenous solution. The label details sodium chloride content (900 mg/100 mL), electrolytes, pH range, storage instructions (20° to 25°C), and manufacturer information (Fresenius Kabi, Lake Zurich, IL, made in Germany). It includes barcode and usage warnings.*
FDA Label Image

Hs (Hs)

Hs (Hs)
A data table listing product numbers, NDC numbers, strength (0.9% or 9 mg/mL), fill sizes, and corresponding bag sizes for 0.9% Sodium Chloride injection solution. Fill sizes range from 50 mL to 1,000 mL with matching bag sizes.*
FDA Label Image
Logo (Logo)
FDA Label Image

Serialized Label (Serialized Label)

Serialized Label (Serialized Label)
A white rectangular label with a barcode and several numeric codes, including (01) 00351662157718 and others. The text instructs to see the manufacturer's package insert and indicates the distributor as HF Acquisition Co., LLC, located in Mukilteo, WA 98275. The label also includes the notation 'RX ONLY' vertically along the right edge.*

* 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.