Potassium Chloride Solution
Product Images NDC 60687-884

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 Chloride (NDC 60687-884). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, 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

20meq Per 15ml Potassium Chloride Oral Solution Cup.jpg (20meq Per 15ml Potassium Chloride Oral Solution Cup)

20meq Per 15ml Potassium Chloride Oral Solution Cup.jpg (20meq Per 15ml Potassium Chloride Oral Solution Cup)
Potassium Chloride Oral Solution USP, 10%, with a dosage of 20 mEq per 15 mL, delivered in a 15 mL volume. The label includes directions to dilute prior to administration and warnings to protect from light and freezing. It features the American Health Packaging logo and states it is for institutional use only.*
FDA Label Image

40meq Per 30ml Potassium Chloride Oral Solution Cup.jpg (40meq Per 30ml Potassium Chloride Oral Solution Cup)

40meq Per 30ml Potassium Chloride Oral Solution Cup.jpg (40meq Per 30ml Potassium Chloride Oral Solution Cup)
Potassium Chloride oral solution label from American Health Packaging, specifying a 10% concentration delivering 40 mEq per 30 mL dose. The label includes instructions to dilute prior to administration and advises protection from light and freezing. The product is for institutional use only with NDC 60687-884-45.*
FDA Label Image

Potassium Chloride Oral Solution Label.jpg (Potassium Chloride Oral Solution Label)

Potassium Chloride Oral Solution Label.jpg (Potassium Chloride Oral Solution Label)
Text panel for Potassium Chloride Oral Solution USP, indicating it is prescription-only and for institutional use only. Instructions include diluting prior to administration and storing between 20° to 25°C with permissible excursions. It advises protection from light and freezing and references USP Controlled Room Temperature guidelines.*

* 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.