Anticoagulant Citrate Phosphate Dextrose (cpd) Blood-pack Units In Pl 146 Plastic Solution
Product Images NDC 0942-9201

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 Anticoagulant Citrate Phosphate Dextrose (cpd) Blood-pack Units In Pl 146 Plastic (NDC 0942-9201). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fenwal, 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.

Product Images & Figures Index

FDA Label Image

4r0837mc Primlbl

4r0837mc Primlbl
Label for Fenwal Blood-Pack Unit Single containing Anticoagulant Citrate Phosphate Dextrose (CPD) Solution, USP. Intended for collection and processing of 250 mL blood with integral donor tube, 16 gauge needle. Manufactured by Fresenius Kabi AG, Germany, made in the US. Includes storage instructions and barcode.*
FDA Label Image

4r0837mcmfg

4r0837mcmfg
Anticoagulant Citrate Phosphate Dextrose (CPD) Blood-Pack Units in PL 146 Plastic, containing CPD solution for intravenous use. The packaging clearly shows the product name, dosage form as solution, and specifies it is for human prescription use. The label identifies Fenwal, Inc. as the manufacturer and lists the NDC code 0942-9201. The product is contained in a transparent flexible plastic blood pack, visible in the image.*
FDA Label Image

Symbols

Symbols
Instructional diagram showing symbols and their meanings for a medical product. Symbols include caution with instructions, steam sterilization, sterile fluid path, non-pyrogenic fluid path, do not reuse, do not vent, reference code, lot number, and orientation arrows labeled 'This way up.'*

* 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.