Zemaira Kit
Product Images NDC 57516-101

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Zemaira (NDC 57516-101). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fisher Clinical Services 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

Zemaira 1000mg Carton (Zemaira 1000mg Carton)

Zemaira 1000mg Carton (Zemaira 1000mg Carton)
Packaging label for ZEMAIRA alpha-1-proteinase inhibitor human kit, an intravenous plasma derivative. The unfolded carton shows the product name, dosage form as a single dose vial with diluent, and 1000 mg range. Manufactured by CSL Behring LLC. Labeler is Fisher Clinical Services Inc. The label includes storage instructions and administration details.*
FDA Label Image

Zemaira 4000mg (Zemaira 4000mg)

Zemaira 4000mg (Zemaira 4000mg)
Packaging label for ZEMAIRA alpha-1-proteinase inhibitor human kit for intravenous administration. The label indicates a 4000 mg range dosage and includes instructions for use and storage. Manufactured by CSL Behring. The label shows the proprietary name ZEMAIRA prominently along with the generic name and dosage details.*
FDA Label Image

Zemaira 500mg (Zemaira 5000mg)

Zemaira 500mg (Zemaira 5000mg)
Packaging label for ZEMAIRA, alpha-1-proteinase inhibitor (human) kit. The label indicates a 5000 mg range for one single-dose vial with diluent. It is for intravenous administration only and is distributed by CSL Behring. The label includes usage and storage instructions, barcode, and the NDC number 0053-7203-02.*

* 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.