Potassium Chloride For Solution
Product Images NDC 40032-194

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 40032-194). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Novel Laboratories, 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

Pouch (5df84b7e 3b09 4249 8c73 A6ec53a14793 01)

Pouch (5df84b7e 3b09 4249 8c73 A6ec53a14793 01)
Label for Potassium Chloride for Oral Solution, USP, containing 20 mEq per single-dose packet of 1.5 g. The label indicates the product is Rx only and manufactured by Novel Laboratories, Inc., Somerset, NJ. Preparation instructions and cautions are included.*
FDA Label Image

Carton-30 Ct (5df84b7e 3b09 4249 8c73 A6ec53a14793 02)

Carton-30 Ct (5df84b7e 3b09 4249 8c73 A6ec53a14793 02)
Packaging label for Potassium Chloride for Oral Solution, USP, 20 mEq strength. The product is orange flavored and comes in 30 single-dose pouches, each containing 1.5 g of Potassium Chloride. The labeler is Novel Laboratories, Inc., Somerset, NJ. The NDC is 40032-194-30.*
FDA Label Image

Carton-100 Ct (5df84b7e 3b09 4249 8c73 A6ec53a14793 03)

Carton-100 Ct (5df84b7e 3b09 4249 8c73 A6ec53a14793 03)
Potassium Chloride for Oral Solution, USP 20 mEq (1.5 g) orange flavored single-dose pouches. The label shows 100 single-dose pouches in the package. Manufactured by Novel Laboratories, Inc. The label includes dosage instructions indicating to dissolve one pouch in 4 ounces of water or other beverage and store at controlled room temperature.*

* 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.