Methylene Blue Injection, Solution
Product Images NDC 0143-9094

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Methylene Blue (NDC 0143-9094). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa 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.

FDA Label Image

Structural Formula (Methylene Blue Injection 1)

Structural Formula (Methylene Blue Injection 1)
Chemical structure of methylene blue showing its molecular framework with dimethylamino groups and a sulfur-containing heterocycle, alongside chloride ion and water of hydration components.*
FDA Label Image

Hikma Logo (Methylene Blue Injection 2)

FDA Label Image

50 mg Per 10 mL Carton Label (Methylene Blue Injection 3)

50 mg Per 10 mL Carton Label (Methylene Blue Injection 3)
Packaging label for Methylene Blue Injection, USP 50 mg per 10 mL (5 mg/mL) intravenous solution by Hikma Pharmaceuticals USA Inc. The label identifies 5 x 10 mL single-dose vials with instructions for slow intravenous injection and use of 5% dextrose injection when diluting. The label includes manufacturer and distributor information, storage instructions, and the NDC 0143-9094.*
FDA Label Image

50 mg Per 10 mL Vial Label (Methylene Blue Injection 4)

50 mg Per 10 mL Vial Label (Methylene Blue Injection 4)
Methylene Blue Injection, USP 50 mg per 10 mL (5 mg/mL) intravenous injection solution. The label indicates it is for intravenous use only and to use 5% Dextrose Injection for dilution. The product is supplied in a 10 mL single-dose vial by Hikma Pharmaceuticals USA Inc., made in the USA.*

* 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.