PureLife APF

Product NDC
68987-014
Requested package NDC
68987-014-15
11-digit product format
689870014
Labeler code
68987
Product ID
68987-014_d5f3f5c7-2f83-2e1c-e053-2995a90a1e8a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Sodium Fluoride
Dosage form
GEL
Route
DENTAL
Labeler
PureLife Dental
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2012-12-18
Substance
SODIUM FLUORIDE
Active strength
5.6 g/454g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
PureLife APF
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SODIUM FLUORIDE5.6 g/454g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
8ZYQ1474W7Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
245593Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
44b91f76-1b7a-40fc-9c80-e1c915b3d2caAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68987-014-15PureLife APF454 g in 1 BOTTLE, PLASTICGEL4544

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68987-014PURELIFE APF (SODIUM FLUORIDE) GEL [PURELIFE DENTAL]4Current NDC, Legacy NDC, 1 package rows20220120_44b91f76-1b7a-40fc-9c80-e1c915b3d2ca.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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
PureLife APFSODIUM FLUORIDEPureLife Dental44b91f76-1b7a-40fc-9c80-e1c915b3d2ca2022-01-19WarningsExact identifier
ndc (package): 68987-014-15
ndc (product): 68987-014
ndc11 (package): 68987001415

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
245593sodium fluoride 2 % Dental GelPSN44b91f76-1b7a-40fc-9c80-e1c915b3d2ca4
245593sodium fluoride 0.02 MG/MG Oral GelSCD44b91f76-1b7a-40fc-9c80-e1c915b3d2ca4
245593sodium fluoride 2 % (fluoride ion 1.23 % ) Dental GelSY44b91f76-1b7a-40fc-9c80-e1c915b3d2ca4
245593sodium fluoride 2.09 % (fluoride ion 1.23 % ) Dental GelSY44b91f76-1b7a-40fc-9c80-e1c915b3d2ca4

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68987-014-1568987001415454 g in 1 BOTTLE, PLASTIC (68987-014-15) 454 g2016-07-010000-00-00NoNoCurrent