Potassium Chloride
Product Images NDC 60505-6185

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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 60505-6185). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Apotex Corp, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Btl10

Btl10
This is a prescription medication with the NDC code of 60505-6184-6. It is manufactured by Apotex Corp. and contains 20 mEq of Potassium Chloride USP per 15 mL. The inactive ingredients include citric acid, glycerin, methylparaben, natural orange flavor, propylene glycol, propylparaben, purified water, sodium citrate, and sucralose. The usual dosage is not given and it is recommended to store the medication in a tight, light-resistant container at controlled room temperature. It is important to keep this medication out of the reach of children.*
FDA Label Image

Btl20

Btl20
This is a description of Potassium Chloride Oral Solution USP, a medication used for electrolyte replenishment. It is available in a 473mL bottle with each 15mL containing 40 mEq of Potassium Chloride USP. The medication should be diluted before use and may contain inactive ingredients such as citric acid, FD&G Yellow #6, glycerin, methylparaben, natural orange flavor, propylene glycol, propylparaben, purified water, sodium citrate, dinydrate, and Sucralose. Usual dosage and prescribing information should be checked before use. It should be stored at room temperature and kept in a tight, light-resistant container. The manufacturer is Apotex Inc. and it is distributed by Apotex Corp.*
FDA Label Image

Crt10

Crt10
FDA Label Image

Crt20

Crt20
This is a medication containing potassium chloride used to treat low levels of potassium in the blood. Each 15 mL (tablespoon) contains 40 mEq of potassium chloride USP that needs to be diluted prior to administration. It also contains inactive ingredients such as citric acid, FDAC Yellow #6, glycerin, methylparaben, natural orange flavor (fruit extract and natural flavor), propylene glycol, propylparaben, purified water, sodium citrate dihydrate, and sucralose. The medication needs to be stored at room temperature and dispensed in a tight, light-resistant container separated from light and freezing. It is manufactured by Apota Inc in Toronto, Ontario, Canada, and distributed by Apotex Corp in Weston, FL 33326. No dosage instructions are provided.*

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