Sodium Chloride Injection, Solution
Product Images NDC 0338-9810

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Sodium Chloride (NDC 0338-9810). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Baxter Healthcare Corporation, 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

Dhcp Letter 1.jpg (Image 01)

A letter dated October 18, 2024, from Baxter Healthcare Corporation addressing the temporary importation of 0.9% Sodium Chloride Injection from Shanghai, China. The letter explains the FDA coordination, product sizes (250 mL, 500 mL, and 1,000 mL), product codes, bags per carton, and NDC codes. It also includes inspection instructions and notes about labels in Chinese with key information in English.*

FDA Label Image

Dhcp Letter 2.jpg (Image 02)

A text document describing key labeling differences and regulatory information for imported 0.9% Sodium Chloride Injection, USP. It discusses compatibility, labeling barcode omissions, prescribing restrictions, and provides contact details for adverse event reporting and product quality issues related to Baxter Healthcare Corporation's product.*

FDA Label Image

Dhcp Letter 3.jpg (Image 03)

FDA Label Image

Dhcp Letter 4.jpg (Image 04)

A product comparison table contrasting FDA-approved 0.9% Sodium Chloride Injection USP and an imported product from Shanghai, China. It outlines differences in label volume, language, indications, active ingredients, pH, storage conditions, container type, and medication port closures, including images of port closures for both products.*

FDA Label Image

Dhcp Letter 5.jpg (Image 05)

This image shows side-by-side representative labels for 0.9% Sodium Chloride Injection USP in 1000 mL intravenous solution form. The left side is the FDA-approved product label in English with dosage and storage information from Baxter Healthcare Corporation. The right side is an imported label from Shanghai, China, featuring similar product details in Chinese and English, including brand name Baxter, concentration 0.9%, and volume 1000 mL.*

FDA Label Image

Dhcp Letter 6.jpg (Image 06)

Sodium Chloride 0.9% Injection in a 1000 mL intravenous solution vial label. The label shows the product name, strength (0.9%), and vial volume (1000 mL). Manufactured by Baxter Healthcare Corporation, it includes storage instructions, batch information fields, and references to package insert details for dosage and precautions.*

FDA Label Image

Sodium Chloride A6c1322 Representative Container Label.jpg (Image 07)

Label of Sodium Chloride Injection 0.9% 250 mL by Baxter Healthcare Corporation. The label includes the proprietary and generic name, dosage form as injection solution, volume of 250 mL, and concentration of 0.9% sodium chloride. Text is primarily in Chinese with some English, indicating intravenous use and single-use instructions.*

FDA Label Image

Sodium Chloride A6c1323 Representative Container Label.jpg (Image 08)

Label for Sodium Chloride Injection, 0.9% strength, 500 mL volume. Text includes product name in Chinese and English, a large "0.9%" concentration indicator, and usage information in Chinese. The label shows it is an intravenous solution, with manufacturer information in Chinese and a lot number and manufacturing details area at the bottom.*

FDA Label Image

Sodium Chloride A6c1324 Representative Container Label.jpg (Image 09)

Sodium Chloride Injection 9 g/1000 mL intravenous solution by Baxter Healthcare Corporation. The label includes volume marking of 1000 mL and concentration of 0.9%. Text is mostly in Chinese with some English, specifying the solution as clear and colorless. Manufacturer details are printed in Chinese with batch and expiration date fields.*

* 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.