Methylene Blue Injection
Product Images NDC 70771-1767

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Methylene Blue (NDC 70771-1767). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Lifesciences Limited, 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

50 mg Per 10 mL Vial (C12095f8 Fb7f 4654 Bcaf E2068297c20d 01)

Methylene Blue Injection USP 5 mg/mL (50 mg/10 mL) single-dose vial label for intravenous use. The label includes dilution instructions using 5% Dextrose Injection and indicates it is a prescription-only product made by Zydus Lifesciences Limited in India.*

FDA Label Image

50 mg Per 10 mL Carton (C12095f8 Fb7f 4654 Bcaf E2068297c20d 02)

Label for Methylene Blue Injection, USP 5 mg/mL (50 mg/10 mL) intravenous injection by Zydus Lifesciences Limited. The label directs use for slow intravenous injection and to use 5% Dextrose Injection when diluting. It specifies a package of 5 single-dose 10 mL vials, with storage instructions and discard warnings. The label design includes color blocks in purple, blue, and teal.*

FDA Label Image

10 mg Per 2 mL Carton (C12095f8 Fb7f 4654 Bcaf E2068297c20d 03)

Packaging label for Methylene Blue Injection, USP 10 mg/2 mL (5 mg/mL) intravenous injection by Zydus Lifesciences Limited. The label indicates it contains 5 single-dose 2 mL vials intended for slow intravenous injection and instructs using 5% Dextrose Injection when diluting. The label includes storage instructions and a barcode.*

* 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.