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 73 of 75 · 1,494 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Ionite APF NeutralSODIUM FLUORIDEDharma Research, inc.ad7a660b-274c-417e-bdf3-1d5addf06ad12020-11-18WarningsExact identifier
unii: 8ZYQ1474W7
Ionite APFSODIUM FLUORIDEDharma Research, inc.8ff1b377-0535-4548-a109-f9f1a43b85b72020-11-16WarningsExact identifier
unii: 8ZYQ1474W7
Ionite APFSODIUM FLUORIDEDharma Research, inc.e6c31330-43e0-4d32-af54-ff852af39cab2020-11-16WarningsExact identifier
unii: 8ZYQ1474W7
Ionite APFSODIUM FLUORIDEDharma Research, inc.bc9664df-c4eb-4d29-b1c0-4d4dff6a75e42020-11-16WarningsExact identifier
unii: 8ZYQ1474W7
Ionite APFSODIUM FLUORIDEDharma Research, inc.b8b7f9b8-ff11-4a76-ab36-7822c15e18922020-11-16WarningsExact identifier
unii: 8ZYQ1474W7
Ionite APFSODIUM FLUORIDEDharma Research, inc.e1797adf-4665-4322-a3aa-dd2da9dcd3a82020-11-16WarningsExact identifier
unii: 8ZYQ1474W7
Ionite APFSODIUM FLUORIDEDharma Research, inc.ce34c159-34cd-47c7-937f-743b3309742b2020-11-16WarningsExact identifier
unii: 8ZYQ1474W7
Ionite APFSODIUM FLUORIDEDharma Research, inc.503ca71a-f50c-4406-b925-5b6ac36a92122020-11-15WarningsExact identifier
unii: 8ZYQ1474W7
Ionite RSODIUM FLUORIDEDharma Research, Inc.1009afc7-6e9d-417f-a702-f8a941e084842020-11-06Warnings, Adverse reactionsExact identifier
unii: 8ZYQ1474W7
Ionite RSODIUM FLUORIDEDharma Research, Inc.0e7b3eb3-3a9e-4a51-b2b5-9f36876fc8a52020-11-06Warnings, Adverse reactionsExact identifier
unii: 8ZYQ1474W7
Ionite APF FoamSODIUM FLUORIDEDharma Research, inc.d22afac7-45d6-467e-951a-e7c241b9180d2020-10-27WarningsExact identifier
unii: 8ZYQ1474W7
Ionite APF FoamSODIUM FLUORIDEDharma Research, inc.4828b482-486f-4105-bed0-3fe2ddbbddb12020-10-27WarningsExact identifier
unii: 8ZYQ1474W7
Ionite APF FoamSODIUM FLUORIDEDharma Research, Inc.8987b447-3fa3-4f52-aecc-80e44c981aaa2020-10-27WarningsExact identifier
unii: 8ZYQ1474W7
Ionite APF NeutralSODIUM FLUORIDEDharma Research, inc.8191554f-adb6-4ba9-aa80-0a9bb65193ec2020-10-27WarningsExact identifier
unii: 8ZYQ1474W7
Ionite APF FoamSODIUM FLUORIDEDharma Research, inc.ddd34623-cb79-4fa7-bd01-19122470b63d2020-10-27WarningsExact identifier
unii: 8ZYQ1474W7
FluoriMax 50001.1% SODIUM FLUORIDE TOOTHPASTEElevate Oral Careae45ae2d-a21f-0a05-e053-2995a90a4d5e2020-09-01WarningsExact identifier
unii: 8ZYQ1474W7
FluoriMax 5000 Sensitive1.1% SODIUM FLUORIDE WITH 5% POTASSIUM NITRATE TOOTHPASTEElevate Oral Careae32b0a2-e42f-6a56-e053-2a95a90a0b002020-08-31WarningsExact identifier
unii: 8ZYQ1474W7
Bach Original Flower RemediesWATERNelson Bach USA Limited09c76050-42c5-4403-865c-a1f6f668d9c02020-06-15WarningsExact identifier
unii: 059QF0KO0R
Sodium Fluoride 5000 ppm SensitiveSODIUM FLUORIDE1.1%, POTASSIUM NITRATE 5%Sheffield Pharmaceuticals LLC02f4cf0b-188c-4522-b759-ffe4a9d150e82020-04-01Warnings, Adverse reactionsExact identifier
unii: 8ZYQ1474W7
Sterile WaterWATERBaxter Healthcare Company8bcf5572-49e1-4302-9522-56f57904cb4a2019-12-29Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

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