Home NDC 73928-021 BRUSH BUDDIES HOTWHEEL ANTICAVITY FLUORIDE STRAWBERRY
Product NDC 73928-021
11-digit product format 739280021
Labeler code 73928
Product ID 73928-021_40b9ee89-d0bf-547c-e063-6294a90ac0f5
Type HUMAN OTC DRUG
Nonproprietary name SODIUM FLUORIDE
Dosage form LIQUID
Route ORAL
Labeler Kingkey MBC Life Technology Group co., LTD.
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-05-10
Substance SODIUM FLUORIDE
Active strength .03 g/100mL
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 BRUSH BUDDIES HOTWHEEL ANTICAVITY FLUORIDE STRAWBERRY
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE .03 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 8ZYQ1474W7 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2682817 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 73928-021-01 BRUSH BUDDIES HOTWHEEL ANTICAVITY FLUORIDE STRAWBERRY 355 mL in 1 BOTTLE LIQUID 355 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73928-021 BRUSH BUDDIES HOTWHEEL ANTICAVITY FLUORIDE STRAWBERRY (SODIUM FLUORIDE) LIQUID [KINGKEY MBC LIFE TECHNOLOGY GROUP CO., LTD.] 1 Current NDC, 1 package rows 20240525_a3e989f8-e6a2-4e13-8faa-77e95895166d.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 5 of 50 · 995 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 73928-021-01 73928002101 355 mL in 1 BOTTLE (73928-021-01) 355 ml 2024-05-10 No No Current