Sodium Chloride Injection
Product Images NDC 0338-0166

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Sodium Chloride (NDC 0338-0166). 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

Assembly 1-3 (Image 01)

Assembly 1-3 (Image 01)
An instructional diagram showing the assembly process for intravenous sodium chloride injection using a drug vial and a Mini-Bag Plus container. Three steps are depicted: removing vial cover and disinfecting stopper; peeling off Mini-Bag foil cover, inspecting adaptor for moisture; and placing vial upright, holding firmly, and pushing adaptor down until vial snaps in place without twisting.*
FDA Label Image

Reconstitution 4-6.jpg (Image 02)

Reconstitution 4-6.jpg (Image 02)
Instructional illustration showing steps 4 to 6 of reconstitution for sodium chloride injection. It demonstrates squeezing the bag to check the vial, breaking the vial seal, holding the bag with vial down to transfer and suspend drug solution, then inverting the bag and squeezing to force air into the vial, with stepwise mixing instructions to ensure the drug is fully dissolved.*
FDA Label Image

List 7 (11)

List 7 (11)
A portion of an instructional text panel detailing the administration steps for intravenous sodium chloride injection. It includes instructions for removing the port protector, hanging the container on an IV pole, priming the set per directions, warnings against using series connections, and guidance on medication administration and disposal of unused portions.*
FDA Label Image

Representative Container Lbl Cb3505005 0338-0160-01 (Image 04)

Representative Container Lbl Cb3505005 0338-0160-01 (Image 04)
Label for a 50 mL vial of 0.9% Sodium Chloride Injection USP, a single-dose container designed for intravenous use with a 13mm vial stopper. The label indicates 450 mg of sodium chloride per 50 mL, manufactured by Baxter Healthcare Corporation. It includes instructions to break the seal and mix before use, storage conditions, and usage warnings.*
FDA Label Image

Representative Container Cb3505006 0338-0164-01 (Image 05)

Representative Container Cb3505006 0338-0164-01 (Image 05)
Label for Sodium Chloride 0.9% Injection USP, 50 mL mini-bag plus single dose container by Baxter Healthcare Corporation. Contains 450 mg sodium chloride per 50 mL, intended for intravenous use. Includes instructions to break seal and mix before use, compatible with 20 mm vial, with storage and handling information. Made in Ireland.*
FDA Label Image

Representative Container Lbl Cb3505007 Ndc 0338-0162-01 (Image 06)

Representative Container Lbl Cb3505007 Ndc 0338-0162-01 (Image 06)
Sodium Chloride 0.9% Injection USP in a 100 mL mini-bag single dose container for intravenous use. The label indicates the strength as 900 mg sodium chloride per 100 mL, in a 13 mm vial. The product is labeled by Baxter Healthcare Corporation, with manufacturing locations in Deerfield, Illinois, USA, and made in Ireland. Storage instructions specify room temperature (25°C) and avoidance of excessive heat.*
FDA Label Image

Representative Container Lbl Cb3505008 0338-0166-01 (Image 07)

Representative Container Lbl Cb3505008 0338-0166-01 (Image 07)
Sodium Chloride 0.9% Injection USP 100 mL intravenous mini-bag single dose container. Contains 900 mg sodium chloride per 100 mL. Label includes storage instructions to keep at room temperature, avoid excess heat, and consult prescribing information. Labeled by Baxter Healthcare Corporation, product made in Ireland with NDC 0338-0166-01.*

* 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.