Home NDC 52257-1470 ATOMY ANTICAVITY TOOTH
Product NDC 52257-1470
11-digit product format 522571470
Labeler code 52257
Product ID 52257-1470_592cacf6-053f-c9c9-e063-6294a90a98a9
Type HUMAN OTC DRUG
Nonproprietary name Sodium Monofluorophosphate
Dosage form PASTE, DENTIFRICE
Route ORAL
Labeler ATOMY CO., LTD.
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-01
Substance SODIUM MONOFLUOROPHOSPHATE
Active strength .76 g/100g
NDC exclude flag No
Listing certified through 2027-12-31
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 ATOMY ANTICAVITY TOOTH
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM MONOFLUOROPHOSPHATE .76 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination C810JCZ56Q Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 545626 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 6 of 51 · 1,013 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 52257-1470-2 52257147002 4 TUBE in 1 CARTON (52257-1470-2) / 50 g in 1 TUBE (52257-1470-1) 4 tube 2026-08-01 No No Current 52257-1470-4 52257147004 1 TUBE in 1 CARTON (52257-1470-4) / 200 g in 1 TUBE (52257-1470-3) 1 tube 2026-08-01 No No Current