Potassium Chloride Solution
Product Images NDC 0603-1542

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 0603-1542). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Endo Usa, 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

Principal Display Panel (20 mEq per 15 mL Bottle Label)

Principal Display Panel (20 mEq per 15 mL Bottle Label)
This is a description of a medication with NDC number 0603-1542-58. The medication is Potassium Chloride Oral Solution, USP, with a strength of 10% and 20 mEq per 15 mL. The medication is manufactured by Ganus Lifesciences Inc. in Allentown, PA and distributed by Par Pharmaceutical in Chestnut Ridge, NY. The medication's GTIN is 00306031542589. Inactive ingredients include citric acid, FDAC Yellow #6, glycerin, natural/artificial orange flavor, purified water, sodium benzoate, sodium citrate dihydrate, and sucralose. The medication must be diluted prior to administration. Dosage and administration information is available in the accompanying prescribing information. The medication should be kept out of the reach of children and stored at 25°C (77°F) with excursions permitted to 16°-30°C (59°-86°F). This medication is only available with a prescription and comes in a 473mL bottle.*
FDA Label Image

Principal Display Panel (40 mEq per 15 mL Bottle Label)

Principal Display Panel (40 mEq per 15 mL Bottle Label)
This is a potassium chloride oral solution medication, manufactured by Ganus Lifesciences Inc. and distributed by Par Pharmaceuticals. It is designed to be diluted prior to administration, and each tablespoon contains 40 mEq of potassium chloride USP at a concentration of 20%. It contains inactive ingredients such as natural/artificial orange flavor, purified water, and sucralose. The prescription medication should be kept away from children, stored at room temperature, protected from light, and freezing. More details on dosage and administration are available in the accompanying prescribing information. The Global Trade Number Identification (GTIN) for this medication is 00306031543586.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.