Alyglo Liquid
Product Images NDC 61476-104

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Alyglo (NDC 61476-104). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gc Biopharma Corp., 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

Principal Display Panelndc 61476-104-01immune Globulinintravenous,human-stwkalyglo10% Liquid (Alyglo 01)

Principal Display Panelndc 61476-104-01immune Globulinintravenous,human-stwkalyglo10% Liquid (Alyglo 01)
Label for Alyglo 10% Liquid, human immunoglobulin G intravenous solution. The label indicates a 5 g/50 mL single-dose vial with 100 mg/mL concentration. It is manufactured by GC Biopharma Corp. and distributed by GC Biopharma USA. It includes storage instructions and lot/expiration date placeholders.*
FDA Label Image

Principal Display Panelndc 61476-104-05immune Globulinintravenous,human-stwkalyglo10% Liquid (Alyglo 02)

Principal Display Panelndc 61476-104-05immune Globulinintravenous,human-stwkalyglo10% Liquid (Alyglo 02)
Packaging label for Alyglo 10% Liquid, an immune globulin intravenous human-stwk product. It is a single-dose vial containing 5 g per 50 mL, solvent/detergent treated and nanofiltered, for intravenous use only. The labeler is GC Biopharma Corp. Storage and handling instructions, along with manufacturer and distributor details, are also included on the label.*
FDA Label Image

Principal Display Panelndc 61476-104-02immune Globulinintravenous,human-stwkalyglo10% Liquid (Alyglo 03)

Principal Display Panelndc 61476-104-02immune Globulinintravenous,human-stwkalyglo10% Liquid (Alyglo 03)
Label for Alyglo 10% Liquid, human immunoglobulin G intravenous solution. The label indicates 10 g per 100 mL in a single-dose vial, solvent/detergent treated, nanofiltered, and Rx only. Manufactured and distributed by GC Biopharma Corp. Storage instructions specify refrigeration and room temperature conditions with expiration placeholders.*
FDA Label Image

Principal Display Panelndc 61476-104-10immune Globulinintravenous,human-stwkalyglo10% Liquid (Alyglo 04)

Principal Display Panelndc 61476-104-10immune Globulinintravenous,human-stwkalyglo10% Liquid (Alyglo 04)
Packaging label for Alyglo 10% Liquid, an intravenous immune globulin product containing 10 g per 100 mL. The label highlights it as human-stwk immune globulin, a plasma derivative for intravenous use only. It is manufactured and distributed by GC Biopharma Corp., with safety storage instructions and product details included.*
FDA Label Image

Principal Display Panelndc 61476-104-03immune Globulinintravenous,human-stwkalyglo10% Liquid (Alyglo 05)

Principal Display Panelndc 61476-104-03immune Globulinintravenous,human-stwkalyglo10% Liquid (Alyglo 05)
Label for Alyglo 10% Liquid, an immune globulin intravenous human plasma derivative containing 20 g per 200 mL (100 mg/mL) solution. The label states single-dose vial, solvent/detergent treated and nanofiltered, for intravenous use only, Rx only. Manufactured by GC Biopharma Corp. Storage and expiration instructions are also included.*
FDA Label Image

Principal Display Panelndc 61476-104-20immune Globulinintravenous,human-stwkalyglo10% Liquid (Alyglo 06)

Principal Display Panelndc 61476-104-20immune Globulinintravenous,human-stwkalyglo10% Liquid (Alyglo 06)
Alyglo 10% Liquid (immune globulin intravenous, human-stwk) packaging label for a 20 g/200 mL single-dose vial. The label indicates the product is solvent/detergent treated and nanofiltered, for intravenous use only, and prescription only. It is manufactured and distributed by GC Biopharma Corp.*

* 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.