Freeflex Logo (Dex1d 0000 01)
Dextrose And Sodium Chloride Injection, Solution
Product Images NDC 63323-869
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Product Visual Gallery
This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Dextrose And Sodium Chloride (NDC 63323-869). 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.
Structural Formula (Dex1d 0000 02)
Fresenius Kabi Logo (Dex1d 0000 03)
Package Label (PRINCIPAL DISPLAY – Dextrose and Sodium Chloride 250 mL Bag Label)
freeflex® is a solution for intravenous use. It contains 5% dextrose and 0.45% sodium chloride, and each 100ml also contains 5g of dextrose hydrous, 450mg of sodium chloride in water for injection for electrolytes per 1000ml. It has a pH of 4.3 and should be used immediately when the seal is broken. While the container is free of natural rubber latex and non-PVG, non-DEHP, and sterile, it may contain some incompatibilities. It should be handled with aseptic technique and the mixing must be thorough. It is made in Germany by Fresenius-kabl.*
Package Label (PRINCIPAL DISPLAY – Dextrose and Sodium Chloride 500 mL Bag Label)
This is a description of a medical product called Free Flex®. It is an injection meant for intravenous use with each 100 mL containing 5g Dextrose, Hydrous and 450 mg Sodium Chloride In water for injection. It also contains Sodium 77 mEq, Chloride 77 mEq and 408 mOsmol/L electrolytes per 1000ml. The package should not be mixed thoroughly and should not be stored until you're ready to use. It is recommended to use the entire container immediately upon removing from the overwrap. It is made in Germany and not made with natural rubber latex. The lot number of this product is (01)00363323869748.*
Package Label (PRINCIPAL DISPLAY – Dextrose and Sodium Chloride 1000 mL Bag Label)
This is a description of a medication with NDC code 63323-869-10 called Free Flex Injection. It is intravenous, Rx only, and contains 5% dextrose and 0.45% sodium chloride in 1000 mL of water for injection. It is a sterile, single-dose container that should not be stored after adding additives. The usual dosage is indicated in the package insert. It is stored at controlled room temperature (20°-25°C). It is made in Germany by Fresenius Kabi. There is an identifier, LOT# 01/0036323869106, and an expiration date. No natural rubber latex or PVC is present in the sterile, non-DEHP container closure. The text also includes a warning about the possible incompatibility of the additives, which should be mixed thoroughly and used aseptically. The text is missing some information such as usage indications and side effects.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
