Potassium Chloride Solution
Product Images NDC 71656-021

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 71656-021). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Saptalis Pharmaceuticals, Llc, 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 (Image00001 V1)

20 Meq Label (Image00001 V1)
This text appears to be an evaluation of a medication labeled as "Potassium Chloride Oral Solution". Each tablespoon (15 mL) of the solution contains 20 milliequivalents (mEq) of potassium chloride. The solution also contains various inactive ingredients such as citric acid, glycerin, flavoring, and preservatives. The usual dosage and prescribing information should be consulted for specific instructions. The solution should be stored within a specific temperature range, protected from light and freezing. It is important to keep this medication out of the reach of children. The National Drug Code (NDC) for this medication is 71656-021-16. The solution is made in the USA.*
FDA Label Image

40 Meq Carton (Image000010 V1)

FDA Label Image

40 Meq Carton (Image000011 V1)

FDA Label Image

20 Meq Label (Image00002 V1)

FDA Label Image

20 Meq Label (Image00003 V1)

20 Meq Label (Image00003 V1)
This is a description of a medication called Potassium Chloride Oral Solution. It is a 10% solution that contains 20 mEq of potassium chloride per 15 mL unit dose cup. The solution has an orange flavor and should be diluted before administration. The medication is only available with a prescription. Each tray contains 50 unit-dose cups. The solution also contains inactive ingredients such as citric acid, FDAC Yellow No. 6, glycerin, methylparaben, natural and artificial orange flavor, propylene glycol, propylparaben, purified water, sodium citrate dihydrate, and sucralose. The medication should be stored at a temperature between 20°C and 25°C (66°F to 77°F) with excursions permitted between 15°C and 30°C (59°F to 86°F). It should be protected from light and freezing. It is important to keep this medication out of reach of children. This medication is for institutional use only and is not child-resistant. The medication is distributed by Saptalis Pharmaceuticals, LLC in Hauppauge, NY.*
FDA Label Image

20 Meq Label (Image00004 V1)

20 Meq Label (Image00004 V1)
This text appears to be the label or description of a medication called Potassium Chloride Oral Solution. The solution contains 10% Potassium Chloride and is intended for oral administration. Each cup of the solution delivers 20 milliequivalents (mEq) of Potassium Chloride in a volume of 15 milliliters (mL). It is flavored with orange and comes in a unit dose packaging. Prior to administration, the solution needs to be diluted. The text also provides information about the ingredients, storage conditions, dosage, and safety precautions. The medication is distributed by Saptalis Pharmaceuticals, LLC in Hauppauge, NY.*
FDA Label Image

40 Meq Label (Image00005 V1)

40 Meq Label (Image00005 V1)
This text appears to be a description of a oral solution called "Potassium Chloride". It contains 10% of potassium chloride and the recommended dosage is 40 mE/30 mL. It is advised to dilute the solution before administration. The packaging is in unit doses of 30 mL with an orange flavor. The product is intended for institutional use only. The name of the manufacturer is "Mig:Saptls Phamaceutcas, LLC" based in Haugpauge, NY.*
FDA Label Image

40 Meq Label (Image00006 V1)

40 Meq Label (Image00006 V1)
This text appears to be a description of a medication called Potassium Chloride Oral Solution USP. It is a 10% solution, with each cup delivering 40 mEq/30 mL. The text mentions that it is important to dilute the solution before administration. The solution has an orange flavor and is meant for oral use only. The text also provides information about the inactive ingredients and storage instructions. It is a prescription-only medication and comes in unit-dose cups, with each tray containing 50 cups. The text also includes safety warnings and information about the manufacturer.*
FDA Label Image

40 Meq Label (Image00007 V1)

40 Meq Label (Image00007 V1)
Description: This is a description of an oral solution of Potassium Chloride with a concentration of 10%, indicated for oral use. Each cup contains 40mEq of potassium chloride in 30mL of solution. The unit-dose packaging delivers 30mL of the solution. The solution has an orange flavor and should be diluted before administration. The product is available in trays containing 10 trays with 100 unit-dose cups each. The solution also contains other inactive ingredients. The recommended dosage and storage instructions are provided. The medication should be kept out of the reach of children and protected from light and freezing. The product is distributed by Sapalis Pharmaceuticals, LLC, located in Hauppauge, NY.*
FDA Label Image

40 Meq Label (Image00008 V1)

FDA Label Image

40 Meq Label (Image00009 V1)

40 Meq Label (Image00009 V1)
This is a description for a potassium chloride oral solution. It is a 20% solution with a concentration of 40 mEqg/15 mL. The solution is delivered in unit doses of 15 mL, and it has an orange flavor. It is intended for institutional use only and is manufactured by Saptals Pharmaceuticals LLC in Hauppauge, NY.*

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