Sodium Chloride Injection, Solution
Product Images NDC 65282-1510

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 Sodium Chloride (NDC 65282-1510). 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.

Product Images & Figures Index

FDA Label Image

Principal Display Panel (5 mL Carton Label)

Principal Display Panel (5 mL Carton Label)
This is a description of two labels of sodium chloride injection in 0.9% concentration, manufactured by Spectra Medical Devices Inc. and BV KL PHARM CO., LTD. The first label has the NOC number 6528215051 and the second one has the NOC number 852821051. The labels have batch and stock numbers as well as manufacturing information for the respective manufacturers.*
FDA Label Image

Principal Display Panel (5 mL Ampule Label)

Principal Display Panel (5 mL Ampule Label)
This is information regarding an injection solution provided in a 5 mL ampule. The solution acts as a sterile diluent and consists of 0.9% sodium chloride. It comes with a prescription and is preservative-free. The solution contains 9 mg of sodium chloride per milliliter and may contain hydrochloric acid or sodium hydroxide for pH adjustment, with a pH range of 4.5 to 7.0. The product is manufactured by KM. Pharm, co., Ltd. in Jecheon, Korea and distributed by Spectra Medical Devices, Inc. in Wilmington, MA. The product code is unknown (XXXX-Y) and should be stored at 20°C to 25°C (68°F to 77°F), with excursions permitted between 15°C and 30°C (59°F to 86°F) at a USP-controlled room temperature. To open the ampule, use gauze and break at the scored neck.*
FDA Label Image

Principal Display Panel (10 mL Carton Label)

Principal Display Panel (10 mL Carton Label)
This is a description of a medication, specifically a 10 mL injection of 0.9% sodium chloride. The injection is preservative free and its NDC code is 6528215101. There are also some coordinates on this page for a location possibly related to the medication.*
FDA Label Image

Principal Display Panel (10 mL Ampule Label)

Principal Display Panel (10 mL Ampule Label)
This text describes a medication called ON 101, which is a sterile diluent used to inject into the body. It comes in a 10 mL Ampule containing 0.9% Sodium Chloride, with a pH range of 4.5 to 7.0. The solution may contain hydrochloric acid and/or sodium hydroxide for pH adjustment. It is manufactured by K.M. Pharm.co., Ltd. in Jecheon, Korea, and is distributed by Spectra Medical Devices, Inc. in Wilmington, MA. ON 101 is used as a preservative-free single-dose injection and is coded as XXXX-Y. It must be stored between 20°C to 25°C (68°F to 77°F), with excursions between 15°C to 30°C (59°F to 86°F) allowed.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.