NDC 72888-024-06 - Potassium Chloride

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 72888-024
Requested NDC: 72888-024-06
Package NDCs from labels: 72888-024-06, 72888-024-07, 72888-024-43, 72888-024-10
Manufacturer: Cardinal Health 107, LLC
Effective date: 2026-08-24
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Potassium Chloride - Cardinal Health 107, LLC	Cardinal Health 107, LLC	2026-08-24	HUMAN PRESCRIPTION DRUG LABEL
Potassium Chloride - Advagen Pharma Limited \| Rubicon Research Limited	Advagen Pharma Limited \| Rubicon Research Limited	2026-01-13	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
72888-024-06	Potassium Chloride	1.58 g in 1 POUCH	POWDER, FOR SOLUTION	1.58	4
72888-024-07	Potassium Chloride	30 in 1 CARTON	POWDER, FOR SOLUTION	30	4
72888-024-10	Potassium Chloride	100 in 1 CARTON	POWDER, FOR SOLUTION	100	4
72888-024-43	Potassium Chloride	50 in 1 CARTON	POWDER, FOR SOLUTION	50	4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72888-024	POTASSIUM CHLORIDE POWDER, FOR SOLUTION [ADVAGEN PHARMA LIMITED]	3	Current NDC, Legacy NDC, 4 package rows	20230307_d528c0c1-b81f-4f7a-8518-e6911b23c3eb.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
72888-024-06	EA - Each	72888-024	6f569bc6-04d5-404a-9477-48d026420ba8	1	2023-02-06
72888-024-07	EA - Each	72888-024	b7dcc393-eb5f-4be8-b60f-280558f498cc	1	2023-02-06
72888-024-10	EA - Each	72888-024	13d7832a-9e46-4885-afcf-ba81c64463db	1	2023-02-06
72888-024-43	EA - Each	72888-024	c1aab91d-4d26-4750-86b8-679f522dc0b8	1	2023-02-06

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 53 of 53 · 1,043 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Join
TIS-U-SOL	SODIUM CHLORIDE, POTASSIUM CHLORIDE, MAGNESIUM SULFATE, SODIUM PHOSPHATE, AND POTASSIUM PHOSPHATE	Baxter Healthcare Corporation	9da4121f-d62d-4da4-8dfb-0494da16015f	2014-02-21	Exact identifier unii: 660YQ98I10
Ringers	SODIUM CHLORIDE, CALCIUM CHLORIDE, POTASSIUM CHLORIDE,	Baxter Healthcare Corporation	e1953d54-818d-46a6-8532-518ebae6d84e	2012-06-13	Exact identifier unii: 660YQ98I10
Lactated Ringers	SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE	Baxter Healthcare Corporation	f09f80bf-2f8b-4420-865d-aec2d5e5cd4d	2012-06-12	Exact identifier unii: 660YQ98I10

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.