Logo (Potassium Phosphate 01)
Potassium Phosphates Injection, Solution, Concentrate
Product Images NDC 0409-0032
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 Potassium Phosphates (NDC 0409-0032). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Hospira, 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
Principal Display Panel – Potassium Phosphates Injection, Usp 15 mL Vial Label (Potassium Phosphate 02)
Label of Potassium Phosphates Injection, USP, 15 mL single-dose vial concentrate for intravenous use by Hospira, Inc. The label states phosphorus content as 45 mmol/15 mL and potassium content as 66 mEq/15 mL. It is preservative-free, nonpyrogenic, and must be diluted before intravenous use. The NDC code 0409-0032-10 is visible along with storage instructions.*
Principal Display Panel – Potassium Phosphates Injection, Usp 15 mL Tray Label (Potassium Phosphate 03)
Packaging label for Potassium Phosphates Injection, USP by Hospira, Inc. It is an intravenous injection concentrate containing dibasic potassium phosphate 236 mg/mL and monobasic potassium phosphate 224 mg/mL. The label indicates a package of 25 single-dose 15 mL vials, with each vial providing phosphorus 4.5 mmol and potassium 6 mEq per 15 mL. It includes storage and usage instructions, highlighting that the solution must be diluted and used intravenously only.*
* 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.
