Magnesium Sulfate Injection, Solution
Product Images NDC 51662-1352

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Magnesium Sulfate (NDC 51662-1352). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, 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

Bag Label (Label)

Label for Magnesium Sulfate Injection, Solution in Water for Injection, 40 mg/mL strength, with a total of 2 g in a 50 mL vial. The label includes dosage information, storage instructions, and handling warnings. The product is labeled by Hospira, Inc., Lake Forest, IL USA, and notes the solution is sterile and nonpyrogenic for intravenous use.*

FDA Label Image

Labeled Bag (Labeled Pouch)

Magnesium Sulfate 40 mg/mL injection solution in a 50 mL flexible plastic IV bag, labeled for intravenous use. The label displays the active ingredient concentration, total 2g per bag, and manufacturer Hospira, Inc. The packaging features a clear fluid container with a port at the bottom for IV administration.*

FDA Label Image

Rfid Label (51662 1352 1 Rfid)

Close-up of a white label on a magnesium sulfate injection solution package from HF Acquisition Co LLC, DBA HealthFirst. The label shows barcode data in parentheses with numbers, a QR code, and text indicating "SEE MANUFACTURE'S INSERT" and distribution details for Mukilteo, WA 98275.*

FDA Label Image

Pouch (51662 1352 2 Pouch Label)

Label for Magnesium Sulfate in water for injection, 2g per 50mL (40mg/mL) in a 50mL bag. The label includes NDC 51662-1352-2, lot number, expiration date, storage instructions, and manufacturer HF Acquisition Co LLC, Mukilteo, WA. It is an intravenous injection, single-dose container. The label states to see the package insert for full information and storage guidelines.*

FDA Label Image

Bag (Bag Label)

Label for Magnesium Sulfate Injection, Solution 2 g/50 mL (40 mg/mL) in water for injection. The label shows it is a single-dose container for intravenous use, supplied by Hospira, Inc., Lake Forest, IL. It states the solution is sterile, nonpyrogenic, and contains DEHP. The label includes dosing instructions and cautions for use.*

FDA Label Image

Case (51662 1352 3 Case Label)

Label for Magnesium Sulfate Injection, Solution, 40 mg/mL strength, in a 50 mL bag. The label states it is a case of 24 bags, manufactured by HF Acquisition Co LLC, DBA HealthFirst. It includes the NDC 51662-1352, lot number, expiration date, usage instructions, and storage information. The route of administration is intravenous.*

FDA Label Image

Rfid Label (51662 1352 3 Updated Rfid)

Partial image of a label for MAGNESIUM SULFATE injection, solution, 40 mg/mL distributed by HF Acquisitions Co LLC, Mukilteo, WA. The label shows linear and 2D barcodes and references the manufacturer's insert for complete information.*

FDA Label Image

Pouch Labeling (Pouch Label 51662 1352 2 Aug 2022)

Label for Magnesium Sulfate in Water for Injection 2 g/50 mL (40 mg/mL) in a 50 mL bag. The label shows the product name, strength, dosage form, NDC 51662-1352-2, lot number, expiration date, manufacturer HF Acquisition Co LLC DBA HealthFirst, and includes detailed usage and storage information for intravenous administration.*

FDA Label Image

Bag Label (Bag Label Aug 2022)

Label for Magnesium Sulfate Injection, Solution, 2 g per 50 mL (40 mg/mL) in water for injection. The label indicates a single-dose 50 mL container marked with HF Acquisition Co LLC, DBA HealthFirst as the distributor. It includes usage instructions, composition details, pH information, and manufacturer name Hospira, Inc.*

* 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.