Home NDC 68987-024-12 NDC 68987-024-12 - 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 68987-024
Requested NDC 68987-024-12
Package NDCs from labels 68987-024-12
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 68987-024-12 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 68987-024 PURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL] 1 1 package rows 20140515_8eae4995-5905-4269-8d53-e7acb54856a3.zip
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded 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 6 of 78 · 1,541 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.