Potassium Chloride Solution
Product Images NDC 53041-680

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Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 53041-680). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Guardian Drug Company, 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

86 (680 473)

86 (680 473)
This is a description of an oral solution medication, with a National Drug Code of 53041-680-06. The dosage and administration are indicated as 56cc, with potassium chloride as an active ingredient and inactive ingredients of citric acid anhydrous, and P t. chl .d el 55, s, mparen. It is important to keep the medication out of reach of children, and to store it at room temperature. The medication should be dispensed in a light-resistant container according to the USP guidelines. The medication is recommended to be diluted before administration and it is available in a 473 mL container. But there is no information about the indications, contraindications, use, benefits, and side effects of the medication.*
FDA Label Image

83 (681 15 Carton)

83 (681 15 Carton)
Potassium Chloride Oral Solution USP, 10% is a medicine for institutional use only. Each unit 15 mL contains 20 milliequivalents of Potassium Chloride. It is prescribed only through a prescription.*
FDA Label Image

83 (681 15)

FDA Label Image

85 (681 30 Carton)

85 (681 30 Carton)
Potassium Chloride Oral Solution USP, 10% is a prescription medication with a concentration of 40 mEq per 30 mL. It comes in a unit dose cup and is manufactured by Guaroun. The National Drug Code for this medication is 53041-681-29. The rest of the text includes some unintelligible characters and numbers, likely due to poor quality.*
FDA Label Image

88 (681 30)

88 (681 30)
This is a description of Potassium Chloride Oral Solution USP, 10%. The solution contains 40 mEq per 30 mL. The packaging instructs to store the solution between 15°-30°C (56”87 2 US Controlled oo temperature) and it is for institutional use only. The package also includes an insert and is only available with a prescription. It was manufactured by G Drug Company located in Cranbury, New Jersey.*
FDA Label Image

87 (681 473)

87 (681 473)
This is a description of a drug called "Potassium Chloride Oral Solution USP." Each tablespoon (15m) of the solution contains 20 mEq of potassium chloride. The dosage and administration information is provided in the accompanying prescribing information. The solution also contains citric acid anhydrous, purified water, and sodium citrate dihydrate. It should be stored in a tight, light-resistant container at a controlled room temperature between 15 and 30°C. The drug is only available with a prescription. The manufacturer's address is provided at the end of the text.*

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