Burkhart

Product NDC
43498-106
11-digit product format
434980106
Labeler code
43498
Product ID
43498-106_d70e56fb-58c7-0593-e053-2a95a90a661a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Sodium Fluoride
Dosage form
GEL
Route
DENTAL
Labeler
Burkhart Dental Supply Inc
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2012-12-14
Substance
SODIUM FLUORIDE
Active strength
5.6 g/454g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
Burkhart
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 SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
5ef9652f-4d99-493d-97ee-9807c6f39182Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43498-106-15Burkhart454 g in 1 BOTTLE, PLASTICGEL4544

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SODIUM FLUORIDEACTIVE INGREDIENT8ZYQ1474W7BURKHART (SODIUM FLUORIDE) GEL [BURKHART DENTAL SUPPLY INC]1
FLUORIDE IONACTIVE MOIETYQ80VPU408OBURKHART (SODIUM FLUORIDE) GEL [BURKHART DENTAL SUPPLY INC]1
CITRIC ACID MONOHYDRATEINACTIVE INGREDIENT2968PHW8QPBURKHART (SODIUM FLUORIDE) GEL [BURKHART DENTAL SUPPLY INC]1
FD&C RED NO. 40INACTIVE INGREDIENTWZB9127XOABURKHART (SODIUM FLUORIDE) GEL [BURKHART DENTAL SUPPLY INC]1
FD&C YELLOW NO. 5INACTIVE INGREDIENTI753WB2F1MBURKHART (SODIUM FLUORIDE) GEL [BURKHART DENTAL SUPPLY INC]1
Magnesium Aluminum SilicateINACTIVE INGREDIENT6M3P64V0NCBURKHART (SODIUM FLUORIDE) GEL [BURKHART DENTAL SUPPLY INC]1
Phosphoric AcidINACTIVE INGREDIENTE4GA8884NNBURKHART (SODIUM FLUORIDE) GEL [BURKHART DENTAL SUPPLY INC]1
Polysorbate 20INACTIVE INGREDIENT7T1F30V5YHBURKHART (SODIUM FLUORIDE) GEL [BURKHART DENTAL SUPPLY INC]1
SACCHARIN SODIUMINACTIVE INGREDIENTSB8ZUX40TYBURKHART (SODIUM FLUORIDE) GEL [BURKHART DENTAL SUPPLY INC]1
Sodium BenzoateINACTIVE INGREDIENTOJ245FE5EUBURKHART (SODIUM FLUORIDE) GEL [BURKHART DENTAL SUPPLY INC]1
Titanium DioxideINACTIVE INGREDIENT15FIX9V2JPBURKHART (SODIUM FLUORIDE) GEL [BURKHART DENTAL SUPPLY INC]1
WaterINACTIVE INGREDIENT059QF0KO0RBURKHART (SODIUM FLUORIDE) GEL [BURKHART DENTAL SUPPLY INC]1
Xanthan GumINACTIVE INGREDIENTTTV12P4NEEBURKHART (SODIUM FLUORIDE) GEL [BURKHART DENTAL SUPPLY INC]1
XylitolINACTIVE INGREDIENTVCQ006KQ1EBURKHART (SODIUM FLUORIDE) GEL [BURKHART DENTAL SUPPLY INC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43498-106BURKHART (SODIUM FLUORIDE) GEL [BURKHART DENTAL SUPPLY INC]4Current NDC, Legacy NDC, 1 package rows20220203_5ef9652f-4d99-493d-97ee-9807c6f39182.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
BurkhartSODIUM FLUORIDEBurkhart Dental Supply Inc5ef9652f-4d99-493d-97ee-9807c6f391822022-02-02WarningsExact identifier
ndc (product): 43498-106

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43498-106-1543498010615454 g in 1 BOTTLE, PLASTIC (43498-106-15) 454 g2013-09-010000-00-00NoNoCurrent