Lactated Ringers Injection, Solution
Product Images NDC 17271-710

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Lactated Ringers (NDC 17271-710). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Becton Dickinson And Company, 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

Freeflex Logo (Bdx0g 0006 01)

LACTATED RINGERS intravenous injection, solution vial. The label displays the product name prominently with the active ingredients sodium chloride, sodium lactate, potassium chloride, calcium chloride. It is manufactured by Becton Dickinson and Company. The vial contains a clear liquid, indicated for intravenous use, consistent with sterile injectable formulation.*

FDA Label Image

Bd Logo (Bdx0g 0006 02)

FDA Label Image

Package Label (PRINCIPAL DISPLAY – Lactated Ringer's Injection, USP 250 mL Bag)

Label for Lactated Ringer's Injection, USP 250 mL intravenous solution by Becton Dickinson and Company. The label details active ingredients per 100 mL: Sodium Chloride 600 mg, Sodium Lactate 310 mg, Potassium Chloride 30 mg, Calcium Chloride 20 mg, with electrolyte concentrations in mEq/L. It is for single use only, with storage instructions and warnings against use in lactic acidosis. The label includes barcode, lot, and expiration placeholders, plus manufacturer information.*

FDA Label Image

Package Label – Principal Display – Lactated Ringer's Injection, Usp 250 mL Shipper (Bdx0g 0006 04)

Label for Lactated Ringer's Injection, USP, 250 mL vial pack of 30, distributed by Becton Dickinson and Company, manufactured by Fresenius Kabi. The label shows storage instructions at 20° to 25°C, lot and expiration date fields, a barcode, and contact information for product inquiries.*

FDA Label Image

Package Label (PRINCIPAL DISPLAY – Lactated Ringer's Injection, USP 500 mL Bag)

Lactated Ringer's Injection, USP 500 mL intravenous solution by Becton Dickinson and Company. The label lists active ingredients per 100 mL: Sodium Chloride 600 mg, Sodium Lactate 310 mg, Potassium Chloride 30 mg, Calcium Chloride 20 mg. It includes storage instructions, usage warnings, and barcodes. The product is single dose only, Rx only, and manufactured by Fresenius Kabi.*

FDA Label Image

Package Label – Principal Display – Lactated Ringer's Injection, Usp 500 mL Shipper (Bdx0g 0006 06)

Label for Lactated Ringer's Injection, USP, 500 mL vial, packaged in a quantity of 20. The label includes storage instructions to keep at 20° to 25°C (68° to 77°F) and to avoid excessive heat. It lists the manufacturer as Fresenius Kabi and the labeler as Becton Dickinson and Company with contact information. NDC 17271-710-06 is shown along with a barcode.*

FDA Label Image

Freeflex Logo (Bdx0g 0006 07)

LACTATED RINGERS intravenous injection, solution, manufactured by Becton Dickinson and Company. The image shows a clear plastic bag with printed label information and a barcode. The bag contains 100 mL of solution, and the product is identified by NDC 17271-710. The label includes details for intravenous administration and handling.*

FDA Label Image

Package Label – Principal Display – Lactated Ringer's Injection, Usp 1000 mL Bag (Bdx0g 0006 08)

Label for Lactated Ringer's Injection, USP, 1,000 mL intravenous solution by Becton Dickinson and Company. Each 100 mL contains Sodium Chloride 600 mg, Sodium Lactate 310 mg, Potassium Chloride 30 mg, and Calcium Chloride 20 mg. Includes storage instructions and proprietary barcodes.*

FDA Label Image

Package Label – Principal Display – Lactated Ringer's Injection, Usp 1000 mL Shipper (Bdx0g 0006 09)

Label for Lactated Ringer's Injection, USP, showing a 1000 mL x 10 quantity package. The label includes storage instructions to keep at 20° to 25°C (68° to 77°F) and avoid excessive heat. It displays the NDC number 17271-710-07 and identifies Becton Dickinson and Company as the distributor, with manufacturing by Fresenius Kabi. The label features a barcode and space for lot and expiration dates.*

* 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.