NDC 72247-101-11 - CURODONT REPAIR FLUORIDE PLUS

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: 72247-101
Requested NDC: 72247-101-11
Package NDCs from labels: 72247-101-11, 72247-101-12
Manufacturer: CREDENTIS AG
Effective date: 2022-01-11
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
CURODONT REPAIR FLUORIDE PLUS - CREDENTIS AG	CREDENTIS AG	2022-01-11	HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
72247-101-12	2023-07-28	C162847	48780-1	0191ceaa-6455-198a-e063-dbdaa90aec3e	CREDENTIS - CURODONT REPAIR FLUORIDE PLUS - MAY CONSULTING

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72247-101-11	CURODONT REPAIR FLUORIDE PLUS	0.1 mL in 1 CYLINDER	SPONGE	0.1		8
72247-101-12	CURODONT REPAIR FLUORIDE PLUS	10 in 1 BOX	SPONGE	10		8

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72247-101	CURODONT REPAIR FLUORIDE PLUS (SODIUM FLUORIDE) SPONGE [CREDENTIS AG]	8	Legacy NDC, 2 package rows	20220115_76207c03-eb76-4c28-8645-ecc13f4aa852.zip

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 26 of 26 · 502 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Eye Wash	WATER	CVS Pharmacy	049cee29-7ec2-4d5b-8308-f522acde43a7	2017-03-29	Warnings	Exact identifier unii: 059QF0KO0R
Sterile Water	WATER	Baxter Healthcare Company	210dc9ab-d6ca-4552-ac19-1be17792d290	2016-05-31	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

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