Potassium Chloride Solution
Product Images NDC 81033-240

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Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 81033-240). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Kesin Pharma Corporation, 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

20 Meq Label (Image0001 Cup)

20 Meq Label (Image0001 Cup)
This text contains information about a medicine called "Potassium Chloride Oral Solution USP, 10%" with an orange flavor in a unit dose delivery of 15 mL. It is manufactured by two pharmaceutical corporations - Dist Kesin Pharma Corporation in Oldsmar, FL, and Mg Saptals Pharmaceuticals, LLC. This medicine is intended for institutional use and comes with the warning that the seal is not child-resistant. The rest of the content in the text is not-readable or not-available due to issues.*
FDA Label Image

20 Meq Label (Image0001)

20 Meq Label (Image0001)
Potassium Chloride Oral Solution is a prescription medicinal product manufactured by Sapalis Pharmaceuticals and distributed by LG Kesin Pharma Corporation. Each cup of the oral solution contains 20mEq of Potassium Chloride USP diluted to a 10% concentration having 15 ml volume, with natural and artificial orange flavor. The unit-dose delivers 15 ml that is to be diluted before administration. The product contains potassium chloride as active medicine and several inactive ingredients such as citric acid anhydrous, FOAC Yellow No. 6, aloyern, mehyiparaben, propylene glycol, propylparaben, purified water, sodium citrate dihydrate, sucrlose, and natural & artificial orange flavor. Potassium Chloride Oral Solution should be stored at 20° to 25°C (68° to 77°F), with excursions permitted between 15°C to 30°C (59°F to 86°F). This medicine must be protected from light and freezing conditions and kept out of the reach of children. The product dosage should be taken as per the accompanying prescription information, and the medicine is only for formal institutional use and not child-resistant.*
FDA Label Image

40 Meq Label (Image0002 Cup)

40 Meq Label (Image0002 Cup)
This is a description of a medication named "Potassium Chloride" in oral solution form, with a potency of 10%. It contains 40 mEq/30 mL and has an orange flavor. The medication is delivered in a unit dose of 30 mL. This particular medication is for institutional use only and is distributed by Kesin Pharma Corporation, Oldsmar, FL, and manufactured by Saptals Pharmaceuticals, LLC. The packaging insert is not child resistant. There is also a unique identification number 8103324030 and a code "Lowanooex Expioct2022 er03224030" which could be an expiration date or a batch code, but it's not clear. The text may have minor errors in spelling and reading.*
FDA Label Image

40 Meq Label (Image0002)

40 Meq Label (Image0002)
This is an oral solution of Potassium Chloride, with a potency of 10% and an orange flavor. It comes in a unit dose of 30 mL, and each tray contains 100 unit-dose cups. Before use, it's necessary to dilute it, and it's only available with a prescription. The inactive ingredients include citric acid anhydrous, FDAC Velow No. 6, gycen, metylparaben, natural, and artificial orange flavors, propylene glycol, propyipaaben, purfed weter, ot citte diydrae, sucraose. For institutional use only. It should be protected from light and freezing and kept away from children. This product is manufactured by Saplali Pharmaceuticals and distributed by Kesin Pharma Corporation in the USA.*

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