NDC 68987-021 - PureLife APF

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: 68987-021
Package NDCs from labels: 68987-021-12
Manufacturer: PureLife Dental
Effective date: 2014-05-14
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
PureLife APF - PureLife Dental	PureLife Dental	2014-05-14	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
68987-021-12	PureLife APF	125 g in 1 BOTTLE, PUMP	AEROSOL, FOAM	125		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68987-021	PURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL]	1	1 package rows	20140516_47ca5997-13e9-478a-b079-a4b6ee4dbf81.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
SODIUM FLUORIDE	ACTIVE INGREDIENT	8ZYQ1474W7	PURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL]	1
FLUORIDE ION	ACTIVE MOIETY	Q80VPU408O	PURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL]	1
HYDROFLUORIC ACID	INACTIVE INGREDIENT	RGL5YE86CZ	PURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL]	1
PHOSPHORIC ACID	INACTIVE INGREDIENT	E4GA8884NN	PURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL]	1
POLOXAMER 407	INACTIVE INGREDIENT	TUF2IVW3M2	PURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL]	1
SACCHARIN SODIUM	INACTIVE INGREDIENT	SB8ZUX40TY	PURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL]	1
SODIUM BENZOATE	INACTIVE INGREDIENT	OJ245FE5EU	PURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL]	1
SODIUM LAURETH-3 SULFATE	INACTIVE INGREDIENT	BPV390UAP0	PURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL]	1
TROLAMINE	INACTIVE INGREDIENT	9O3K93S3TK	PURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL]	1
Water	INACTIVE INGREDIENT	059QF0KO0R	PURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL]	1
XYLITOL	INACTIVE INGREDIENT	VCQ006KQ1E	PURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL]	1

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 78 of 78 · 1,541 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
5198f457-335d-4559-9bad-366c3c2923f5			47ca5997-13e9-478a-b079-a4b6ee4dbf81	2014-05-14	Warnings	Exact identifier spl id: 5198f457-335d-4559-9bad-366c3c2923f5 spl set id: 47ca5997-13e9-478a-b079-a4b6ee4dbf81

Reported adverse events (FAERS/openFDA)#

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