Potassium Chloride
Product Images NDC 21695-712

2 FDA label images from Rebel Distributors Corp · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 21695-712). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rebel Distributors 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

Potassium Chloride 10meq K (Aa6d9e02 0ff8 421d 9ddd 8968f41f0af7 01)

Potassium Chloride 10meq K (Aa6d9e02 0ff8 421d 9ddd 8968f41f0af7 01)
Potassium Chloride 10 mEq K ER Tablets label showing the active ingredient as Potassium Chloride 750 mg per extended-release tablet. The label includes the product ID PP071190 and indicates it is packaged by Physician Partner, a division of Rebel Distributors Corp. It features dosage form information, storage instructions at 15° to 30°C (59° to 86°F), and caution to keep medication out of children’s reach. Manufacturer is Watson Laboratories, Inc., Corona, CA.*
FDA Label Image

Potassium Chloride 1,500mg (20meqk (Aa6d9e02 0ff8 421d 9ddd 8968f41f0af7 02)

Potassium Chloride 1,500mg (20meqk (Aa6d9e02 0ff8 421d 9ddd 8968f41f0af7 02)
Potassium Chloride 1,500 mg (20 mEq) ER Tablets label from Physician Partner, with NDC 21695-712-30. The label indicates each extended-release tablet contains potassium chloride equivalent to 20 mEq of potassium. The product is packaged by Physician Partner in Thousand Oaks, CA, and includes storage instructions at controlled room temperature (15°-30°C/59°-86°F). The label shows quantity (#30 tablets) and specifies RX 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.