FDA.reportPublic FDA data

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
LabelManufacturerEffective dateType
PureLife APF - PureLife DentalPureLife Dental2014-05-14HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68987-024-12PureLife APF125 g in 1 BOTTLE, PUMPAEROSOL, FOAM1251

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68987-024PURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL]11 package rows20140515_8eae4995-5905-4269-8d53-e7acb54856a3.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SODIUM FLUORIDEACTIVE INGREDIENT8ZYQ1474W7PURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL]1
FLUORIDE IONACTIVE MOIETYQ80VPU408OPURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL]1
HYDROFLUORIC ACIDINACTIVE INGREDIENTRGL5YE86CZPURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL]1
PHOSPHORIC ACIDINACTIVE INGREDIENTE4GA8884NNPURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL]1
POLOXAMER 407INACTIVE INGREDIENTTUF2IVW3M2PURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL]1
SACCHARIN SODIUMINACTIVE INGREDIENTSB8ZUX40TYPURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL]1
SODIUM BENZOATEINACTIVE INGREDIENTOJ245FE5EUPURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL]1
SODIUM LAURETH-3 SULFATEINACTIVE INGREDIENTBPV390UAP0PURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL]1
TROLAMINEINACTIVE INGREDIENT9O3K93S3TKPURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL]1
WaterINACTIVE INGREDIENT059QF0KO0RPURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL]1
XYLITOLINACTIVE INGREDIENTVCQ006KQ1EPURELIFE 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 37 of 76 · 1,509 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sodium Fluoride ChewableSODIUM FLUORIDEBryant Ranch Prepackce6968ce-30ee-48d5-8648-52b4efd38fe82025-11-13Warnings, Adverse reactionsExact identifier
unii: 8ZYQ1474W7
Allday 5000 Sensitive1.1% SODIUM FLUORIDE TOOTHPASTEElevate Oral Care401f5e96-095b-c001-e063-6394a90ab55e2025-11-12WarningsExact identifier
unii: 8ZYQ1474W7
Dr Tichenors With Extra Whitening and Tartar ControlSODIUM FLUORIDEDr. G. H. Tichenor's Antiseptic Companybce596e8-07eb-4e56-9007-9d283e14372d2025-11-12WarningsExact identifier
unii: 8ZYQ1474W7
Quality Choice Natural WhiteFLUORIDECHAIN DRUG MARKETING ASSOCIATION INC8d187823-7e56-441b-8bca-8f03e7bb07c72025-11-12WarningsExact identifier
unii: 8ZYQ1474W7
Natural Relief Diarrhea ReliefALOE, CITRULLUS COLOCYNTHIS, CROTON TIGLIUM, LYCOPODIUM CLAVATUM, MAGNESIUM SULFATE HEPTAHYDRATE, PHOSPHORIC ACID, THUJA OCCIDENTALISTRP Company436de0c5-acd6-e32b-e063-6394a90aa2752025-11-12WarningsExact identifier
unii: E4GA8884NN
Sodium Fluoride ChewableSODIUM FLUORIDEBryant Ranch Prepackbe789a6f-b4b4-4088-aaeb-bcbc6ae1e33b2025-11-12Warnings, Adverse reactionsExact identifier
unii: 8ZYQ1474W7
Super Chocolate PrescriptionANTICAVITY TOOTHPASTESuperMouth, LLC.bbaccbe4-82ac-4c51-8fc4-a96bf86dfef22025-11-12WarningsExact identifier
unii: 8ZYQ1474W7
Eyesaline Eyewash ConcentratePURIFIED WATERHoneywell Safety Products USA, Inc.3765c251-eb14-d60f-e063-6294a90a6a4d2025-11-12WarningsExact identifier
unii: 059QF0KO0R
Eyesaline Emergency EyewashPURIFIED WATERHoneywell Safety Products USA, Inc.37f244fd-c02f-e66a-e063-6394a90aed812025-11-12WarningsExact identifier
unii: 059QF0KO0R
Super Mint PrescriptionANTICAVITY TOOTHPASTESuperMouth, LLC.6773eb58-93b0-4e86-b780-7dde378c0bc32025-11-12WarningsExact identifier
unii: 8ZYQ1474W7
Spry DentifriceTOOTHPASTEXlear Inc.43567bbc-b07e-b605-e063-6294a90aad782025-11-11WarningsExact identifier
unii: 8ZYQ1474W7
Anti Nausea LiquidPHOSPHORATED CARBOHYDRATETOPCO ASSOCIATES LLCfd0e8feb-89b5-42ff-806a-55b7473cf5872025-11-10WarningsExact identifier
unii: E4GA8884NN
Super MintMINT TOOTHPASTESuperMouth, LLC.d23e89f5-7b65-4ed9-803a-38233f30d8f22025-11-07WarningsExact identifier
unii: 8ZYQ1474W7
STERILE WATERWATERHenry Schein, Inc.f4087143-9868-4308-b96c-43657ee8ec282025-11-07Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
PCXX CREME DE MENTHE APF GSODIUM FLUORIDERoss Healthcare Inc.8281bc97-3816-8653-e053-2991aa0a0f502025-11-06Exact identifier
unii: 8ZYQ1474W7
PCXX GRAPE APF GSODIUM FLUORIDERoss Healthcare Inc.82872a07-04b7-5263-e053-2a91aa0aa2c22025-11-06Exact identifier
unii: 8ZYQ1474W7
PCXX VANILLA ORANGE NEUTRAL GLSODIUM FLUORIDERoss Healthcare Inc.82978289-4943-83b1-e053-2991aa0a63652025-11-06Exact identifier
unii: 8ZYQ1474W7
PCXX NEUTRAL RNS GRAPEFLUORIDE TREATMENTRoss Healthcare Inc.9c40dff1-ff82-44b3-98e5-7f9cbfd1dad62025-11-06WarningsExact identifier
unii: 8ZYQ1474W7
PCXX NEUTRAL RMS BUBBLEGUMFLUORIDE TREATMENTRoss Healthcare Inc.37f90a0f-2c67-456b-997e-8a8a4f5f09d32025-11-06WarningsExact identifier
unii: 8ZYQ1474W7
PCXX NEUTRAL RNS PEPPERMINTFLUORIDE TREATMENTRoss Healthcare Inc.8532d4d9-c960-0051-e053-2a91aa0ad1a62025-11-06WarningsExact identifier
unii: 8ZYQ1474W7

Reported adverse events (FAERS/openFDA)#

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