Home NDC 51009-921 TOMS OF MAINE WHITEN PLUS DEEP CLEAN SPEARMINT
Product NDC 51009-921
11-digit product format 510090921
Labeler code 51009
Product ID 51009-921_e01ecaef-cd8c-4bb4-83f5-f8e7eb55469c
Type HUMAN OTC DRUG
Nonproprietary name Sodium Fluoride
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler Tom's of Maine, Inc.
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-01-01
Substance SODIUM FLUORIDE
Active strength 1.1 mg/g
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 TOMS OF MAINE WHITEN PLUS DEEP CLEAN SPEARMINT
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE 1.1 mg/g
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 416783 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 51009-921-40 Toms of Maine Deep Clean Spearmint 1 in 1 CARTON PASTE, DENTIFRICE 1 1 51009-921-40 Toms of Maine Deep Clean Spearmint 113 g in 1 TUBE PASTE, DENTIFRICE 113 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 51009-921 TOMS OF MAINE DEEP CLEAN SPEARMINT (SODIUM FLUORIDE) PASTE, DENTIFRICE [TOM'S OF MAINE] 1 Current NDC, 2 package rows 20250101_1fe50b49-bc62-4137-866c-e87bb878a96d.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 51009-921-40 51009092140 1 TUBE in 1 CARTON (51009-921-40) / 113 g in 1 TUBE 1 tube 2025-01-01 No No Current