Magnesium Sulfate
Product Images NDC 51662-1451

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Magnesium Sulfate (NDC 51662-1451). 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

Dosage (Dosage)

A data table listing substances or compounds, including Alcohol (in high concentrations), Alkali carbonates and bicarbonates, Alkali hydroxides, Arsenates, Barium, Calcium, Clindamycin phosphate, Heavy metals, Hydrocortisone sodium succinate, Phosphates, Polymyxin B sulfate, Procaine hydrochloride, Salicylates, Strontium, and Tartrates.*

FDA Label Image

How Supplied (How Supplied)

A data table listing several product variations of magnesium sulfate heptahydrate with details including NDC numbers, concentration of 500 mg/mL, fill volumes ranging from 2 mL to 10 mL, magnesium content of 49.3 mg/mL, and sulfate content of 194.7 mg/mL.*

FDA Label Image

Logo (Logo)

FDA Label Image

Vial Label (New Vial Label)

Packaging label for Magnesium Sulfate Injection, USP, 50% strength, containing 5 grams per 10 mL (500 mg per mL) in a 10 mL single dose vial. The label indicates the product is preservative free, for intramuscular or intravenous use with a note that it must be diluted before intravenous use. Manufactured by Fresenius Kabi, Lake Zurich, IL.*

FDA Label Image

Serialized Label (Serialized Label)

MAGNESIUM SULFATE Injection, USP 50% strength in a 10 mL single dose vial. The label shows it contains 5 grams per 10 mL (500 mg per mL), is preservative-free, and is for intramuscular or intravenous use after dilution. Distributed by HF Acquisition Co LLC, DBA HealthFirst.*

FDA Label Image

Vial 3rd Part (Vial 3rd Part)

Label for MAGNESIUM SULFATE injection by HF Acquisition Co LLC, DBA HealthFirst. The label includes lot number 403340 and expiration date 08/20. It also shows the manufacturer Fresenius Kabi Lake Zurich, IL 60047, and includes a barcode.*

FDA Label Image

Vial 1st Part (Vial Label 1st Part)

Magnesium Sulfate Injection, USP 50% (5 grams per 10 mL) vial label showing product strength, dosage form as injection, preservative free single dose vial of 10 mL, with usage notes for intramuscular or intravenous use and a warning that it must be diluted before intravenous use.*

FDA Label Image

Vial 2nd Part (Vial Label 2nd Part)

A drug label panel for Magnesium Sulfate injectable solution. It lists the active ingredient as magnesium sulfate heptahydrate 500 mg per mL, along with water for injection and possible additives for pH adjustment. It states magnesium content equivalence and osmolarity, aluminum limit, typical dosage reference, storage instructions at 20° to 25°C, and note to discard unused solution and ensure clarity and seal before use.*

* 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.