Sodium Chloride Injection, Solution
Product Images NDC 65282-1505

4 FDA label images from Spectra Medical Deviecs, Llc · 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 Sodium Chloride (NDC 65282-1505). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Spectra Medical Deviecs, 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

Principal Display Panel (5 mL Carton Label)

Principal Display Panel (5 mL Carton Label)
Packaging label for Sodium Chloride 0.9% Injection, USP, 9 mg/mL solution in 5 mL single-dose ampules. The label indicates it is preservative-free and manufactured by Spectra Medical Devices, Inc. It includes storage instructions and states the product is for use as a sterile diluent. The label shows the NDC code 65822-1505-1 and mentions the product is for intramuscular, intravenous, and subcutaneous routes.*
FDA Label Image

Principal Display Panel (5 mL Ampule Label)

Principal Display Panel (5 mL Ampule Label)
Label of Sodium Chloride 0.9% Injection, USP 5 mL ampule by Spectra Medical Devices, LLC. The sterile single-dose solution contains 9 mg/mL sodium chloride, preservative-free, used as a sterile diluent with a pH adjusted between 4.5 and 7.0. Manufactured by Spectra Medical Devices, Inc., Wilmington, MA and K.M. Pharm. Co., Ltd., Jecheon, Korea. The label includes a barcode, storage instructions, lot number, and expiration date fields.*
FDA Label Image

Principal Display Panel (10 mL Carton Label)

Principal Display Panel (10 mL Carton Label)
Label for 0.9% Sodium Chloride Injection, USP, 10 mL single-dose ampules. The label shows the drug strength as 9 mg per mL in water for injection. It is preservative-free and intended as a sterile diluent. Manufactured by Spectra Medical Devices, Inc., with additional manufacture by K.M. Pharm Co., Ltd. The label includes storage instructions and a barcode.*
FDA Label Image

Principal Display Panel (10 mL Ampule Label)

Principal Display Panel (10 mL Ampule Label)
Packaging label of Sodium Chloride Injection, USP 10 mL ampule, 0.9% (9 mg/mL) solution, preservative-free, for use as a sterile diluent. Manufactured for Spectra Medical Devices, Inc. The label shows storage instructions, single-dose use, and distributor information.*

* 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.