Dextrose And Sodium Chloride Injection, Solution
Product Images NDC 63323-867
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This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Dextrose And Sodium Chloride (NDC 63323-867). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Fresenius Kabi Usa, 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
Structural Formula (Dex1a 0000 02)
Fresenius Kabi Logo (Dex1a 0000 03)
Freeflex Logo (Dex1a 0000 04)
Package Label (PRINCIPAL DISPLAY – Dextrose and Sodium Chloride 250 mL Bag Label)
This text describes a medication with the National Drug Code (NDC) 63323-867-75, called "freeflex® 250 mL". It is an intravenous solution containing 5% Dextrose and 0.3% Sodium Chloride, used for medical purposes only. One package contains 100 single-dose containers that need to be discarded if unused, and any additions to this medication should be checked with a pharmacist for compatibility. The medication needs to be stored at a temperature between 20°C to 25°C, protected from freezing. This solution has electrolytes such as Sodium and Chloride in each 100 mL, and the container closure is made without natural rubber latex. The rest of the information in the text is related to the composition, dosage, and storage of this medication.*
Freeflex Logo (Dex1a 0000 06)
Package Label (PRINCIPAL DISPLAY – Dextrose and Sodium Chloride 500 mL Bag Label)
This is a description for a prescription-only intravenous solution with the following specifications: 5% Dextrose and 0.3% Sodium Chloride Injection, USP, 2500 mL, with the electrolyte composition of Sodium 51 mEq; Chloride 51 mEq per 1000 mL. Its components include Dextrose, Hydrous, and Sodium Chloride, and has a pH of 4.3. The solution comes in a single-dose container and should be used immediately once removed from its overwrap. It is advised to consult a pharmacist before administering any incompatible additives, and to use an aseptic technique upon doing so. The container closure is not made of natural rubber latex, Non-PVC, Non-DEHR Sterile. Store at a controlled room temperature, and manufacture sites are located in Germany with a distributor center in Lake Zurich.*
Freeflex Logo (Dex1a 0000 08)
Package Label (PRINCIPAL DISPLAY – Dextrose and Sodium Chloride 1000 mL Bag Label)
This is a description of a medication called "5% Dextrose and 0.3% Sodium Chloride Injection, USP" designed for intravenous use. The medication is contained within a 1000 mL bottle and is made up of a 5g mixture of dextrose and hydrous plus 300mg of sodium chloride in water for injection. The solution has a pH of 4.3 and a 355 mOsmol/L concentration. The medication is designed for single use only and any unused portions should be discarded. It is not recommended to introduce any additives and if needed one should consult with their physician. The ideal storage temperature is between 20 to 25°C and should be protected from freezing. Also, the container closure is not made with natural rubber latex, and the medication is non-PVC, non-DEHP, and sterile. However, there is no information regarding the recommended dosage and how to use the medication.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.