Chemical Structure (Dextrose And Sodium Chloride Injection Usp 1)
Dextrose And Sodium Chloride Injection, Solution
Product Images NDC 0264-7614
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Product Visual Gallery
This gallery contains 29 technical images submitted to the FDA as part of the official labeling for Dextrose And Sodium Chloride (NDC 0264-7614). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by B. Braun Medical Inc., 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
Other (Dextrose And Sodium Chloride Injection Usp 10)
500 mL Container Label L6101 (Dextrose And Sodium Chloride Injection Usp 11)
This is a description of a medical product, specifically an injection solution for intravenous use. It is a combination of Dextrose and Sodium Chloride in a 5% and 0.45% concentration respectively. Each 100 mL contains 5g of hydrous Dextrose USP and 0.45g of Sodium Chloride USP with pH at 4.4 and electrolytes (mEq/liter) of Na-77 and Cl-77. The solution is sterile, nonpyrogenic and is contained in a single dose container. The recommended storage temperature is room temperature (25°C), and it should be protected from excessive heat and freezing. The container should not be used if the seals have been broken, and minute leaks should be checked before use. The barcode is provided for tracking and distribution purposes. Some additives may be incompatible, and a pharmacist should be consulted before adding them. The product is distributed by B. Braun Medical Inc. and is Rx only.*
Other (Dextrose And Sodium Chloride Injection Usp 12)
1000 mL Container Label L6120 (Dextrose And Sodium Chloride Injection Usp 13)
This is a description of a pharmaceutical product called "5% Dextrose and 0.45% Sodium Chloride Injection USP". Each 100mL of the product contains 5g of hydrous dextrose USP, 0.45g of Sodium Chloride USP and water for injection USP qs. The product is hypertonic and has a pH of 4.4 (3.5-6.5) and an osmolarity of 405 mOsmolfliter. It has a recommended storage temperature of room temperature at 25°C and should be protected from excessive heat and freezing. It comes in a 500mL EXCEL® container that is sterile and nonpyrogenic, and a single dose container that should not be used in series connection. The product has warnings that some additives may be incompatible and one should consult with a pharmacist before introducing additives using aseptic techniques. It should not be stored after mixing and is not made with natural rubber latex, PUC, or DEHP.*
Other (Dextrose And Sodium Chloride Injection Usp 14)
500 mL Container Label L6121 (Dextrose And Sodium Chloride Injection Usp 15)
This is a description of a medical product called "5% Dextrose and 0.45% Sodium Chloride Injection USP". It comes in a 250 mL DXETT® container with the NDQ code of 0264-7612-20 and the lot number of L6122. Each 100mL of the product contains Hydrous Dextrose USP, Sodium Chloride USP, and water for injection with pH of 4.4 and osmolarity of 408 mOsmol/liter. It is a hypertonic solution that contains electrolytes such as Na+ and Cl-. The warning advises to use the product only when it is free of any presence of leaks and other abnormalities.*
Other (Dextrose And Sodium Chloride Injection Usp 16)
250 mL Container Label L6122 (Dextrose And Sodium Chloride Injection Usp 17)
This is a 1000 mL single dose container of 5% Dextrose and 0.33% Sodium Chloride Injection USP. Each 100 mL of the solution contains 5g of hydrous dextrose USP, 0.33 of sodium chloride USP, and water for injection USP. The pH is 4.4 (3.5-6.5), and the calculated osmolarity is 365 mOsmol/L, hypertonic. The electrolyte levels (mEq/L) are sodium (Na) 56 and chloride (CI) 56. The solution is sterile, nonpyrogenic and for intravenous use only. It is not recommended to administer simultaneously with blood or other incompatible additives. It should not be stored with natural rubber latex, PVC, or DEHP. Recommended storage is at room temperature. The container and seals must be clear to use. This solution is made by B. Braun Medical Inc.*
Other (Dextrose And Sodium Chloride Injection Usp 18)
500 mL Container Label L6140 (Dextrose And Sodium Chloride Injection Usp 19)
This is a description of a medical product - an injection solution containing 5% Dextrose and 0.33% Sodium Chloride, available in a 500 ml Excel container. The product has a single-use container, must be used intravenously, and is sterile and non-pyrogenic. The solution has an electrolyte balance of 56mEq/liter of Na+ and 58mEq/liter of Cl-. The product must be stored at 25°C and should be protected from excessive heat. The product should not be used if there are any leaks found and is not suitable for people with impaired safety. The product is not made of natural rubber and has a barcode for easy identification. The description does not mention what the injection is used for.*
Other (Dextrose And Sodium Chloride Injection Usp 2)
Other (Dextrose And Sodium Chloride Injection Usp 20)
500 mL Container Label L6141 (Dextrose And Sodium Chloride Injection Usp 21)
This is a description of a solution for intravenous use that contains 5% dextrose and 0.20% sodium chloride. It is a sterile, nonpyrogenic single-dose container with electrolytes and hydrous dextrose. The solution should be used for intravenous use only, and caution is recommended when introducing additives. The solution should be stored at room temperature and should not be used simultaneously with blood. The container should be checked for minute leaks and discarded if found. The solution is made without natural rubber latex, PVC, or DEHP.*
Other (Dextrose And Sodium Chloride Injection Usp 22)
1000 mL Container Label L6160 (Dextrose And Sodium Chloride Injection Usp 23)
This is a description of a medical product called "5% Dextrose and 0.20% Sodium Chloride Injection USP". It comes in a 500mL Excel container with a pH of 4.4 (3.5-6.5) and an osmolarity of 320 mOsmal/fliter. Each 100mL contains Hydrous Dextrose USP 5g, Sodium Chloride USP 0.2g, and Water for Injection USP. It also contains electrolytes with Na at 34 mEg/lite and CI at 34 mEg/lite. There is a barcode on the product and it is for Rx only.*
Other (Dextrose And Sodium Chloride Injection Usp 24)
500 mL Container Label L6161 (Dextrose And Sodium Chloride Injection Usp 25)
Other (Dextrose And Sodium Chloride Injection Usp 26)
250 mL Container Label L6162 (Dextrose And Sodium Chloride Injection Usp 27)
The text provides information about a 1000 mL sterile, nonpyrogenic, and single-dose intravenous solution with 10% dextrose and 0.45% sodium chloride. The solution is hypertonic and has a pH of 4.3 and an osmolarity of 660 mOsmol/liter. It contains Na and Cl electrolytes in 77 mEq/liter each. The container is an EXCEL® container with reference number 16220 and NDC number 0264-7622-00. The solution is not compatible with some additives, and it should be stored at room temperature and safeguarded from freezing. The package should not be opened until ready to use, and the solution should be discarded if the container appears to be leaking. The solution is free from natural rubber latex, PVC, or DEHP. The text also provides manufacturer and contact information for B. Braun Medical Inc.*
Other (Dextrose And Sodium Chloride Injection Usp 28)
1000 mL Container Label L6220 (Dextrose And Sodium Chloride Injection Usp 29)
This text describes a medication called 10% Dextrose and 0.20% Sodium Chloride Injection, which is packaged in a DETT container labeled with the product code 0264-7623-20. Each 100mL of this medication contains 10 grams of Hydraus Dextrose USP and 0.2 grams of Sodium Chloride USP. The medication is hypertonic and has an osmolarity of 575 mOsmol/liter. Additionally, it contains electrolytes, including 34 mEq/L of both sodium and chloride ions. There is a caution to store the medication at room temperature and avoid freezing. The text also includes a barcode and lot number for quality control purposes.*
1000 mL Container Label L6050 (Dextrose And Sodium Chloride Injection Usp 3)
This is a description of a solution for intravenous use only, containing 3.3% Dextrose and 0.30% Sodium Chloride. Each 100 mL vial contains 3.3 g of hydrous dextrose, 0.3 g of Sodium Chloride, and Water for Injection. The solution has a pH range of 4.5 (3.5-6.5) with a calculated Osmolarity of 270 mOsmol/liter. It is a sterile, non-pyrogenic, and single-dose container. The recommended storage temperature is below 25°C, and the solution should be protected from freezing. It is not compatible with blood so avoid administering simultaneously. Minute leaks can impair sterility, so check for leakages before use. The solution should not be used after the expiration date. There is a warning about adding other additives and mixing them thoroughly before use.*
Other (Dextrose And Sodium Chloride Injection Usp 4)
1000 mL Container Label L6080-00 (Dextrose And Sodium Chloride Injection Usp 5)
This is a description of a sterile solution for intravenous use. The solution contains 3.3% dextrose and 0.30% sodium chloride in water for injection. It has a pH range of 3.5-6.5 and an osmolarity of 270 mOsmol/L. The container is a single-dose sterile Excel container that should not be used in series connection. The solution should be used as soon as it is clear, and containers/seals are intact. Additives should be introduced using aseptic techniques. Storage should be at room temperature, and the solution should be protected from excessive heat. After removing the overwrap, check for minute leaks by squeezing the container, and if leaks are found, discard the solution. It is made by Braun Medical Inc.*
Other (Dextrose And Sodium Chloride Injection Usp 6)
500 mL Container Label L6081-00 (Dextrose And Sodium Chloride Injection Usp 7)
This is a sterile, nonpyrogenic solution for intravenous use containing 5% Dextrose and 0.9% Sodium Chloride. Each 100 mL contains 5 g of Hydrous Dextrose USP and 0.9 g of Sodium Chloride USP. It is a single-dose container to be used only if the solution is clear, container and seals are intact, and not to be used in a series connection. It is recommended to store it at room temperature, protect from freezing and not to use if the overwrap shows signs of damage. The Electrolytes (mEq/liter) contain Na* 154 and CI~ 154. Additives may be incompatible, and a pharmacist should be consulted before introducing them, and aseptic techniques should be used when doing so. It is not made with natural rubber latex, PVC, or DEHP. It is Rx only.*
Other (Dextrose And Sodium Chloride Injection Usp 8)
1000 mL Container Label L6100 (Dextrose And Sodium Chloride Injection Usp 9)
This is a description of a 500mL container of 5% Dextrose and 0.9% Sodium Chloride Injection USP. The injection contains Sodium Chloride USP and Hydrous Dextrose USP. The pH of the injection is 4.4 with an osmolarity of 560mOsmol/liter, making it hypertonic. The Sterile injection is non-pyrogenic and is for intravenous use only. The container should not be used if the solution is not clear, or the seals are broken. Additives must be compatible and only added with aseptic techniques. Not available for storage instructions. The container should not be removed from the wrapper if it's not ready for use, and if there are leaks found upon unwrapping, the solution must be discarded. The product is Rx only and does not contain natural rubber, nor AC or DEHP.*
* 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.
