Home NDC 51009-920 Toms of Maine Whiten Plus Deep Clean Peppermint
Product NDC 51009-920
11-digit product format 510090920
Labeler code 51009
Product ID 51009-920_ecb6dca1-5bf7-4097-b825-e63cbc7d88fd
Type HUMAN OTC DRUG
Nonproprietary name Sodium Fluoride
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler Tom's of Maine
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 Peppermint
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 51009-920-40 Toms of Maine Whiten Plus Deep Clean Peppermint 1 in 1 CARTON PASTE, DENTIFRICE 1 4 51009-920-40 Toms of Maine Whiten Plus Deep Clean Peppermint 113 g in 1 TUBE PASTE, DENTIFRICE 113 4 51009-920-63 Toms of Maine Whiten Plus Deep Clean Peppermint 85 g in 1 TUBE PASTE, DENTIFRICE 85 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 51009-920 TOMS OF MAINE WHITEN PLUS DEEP CLEAN PEPPERMINT (SODIUM FLUORIDE) PASTE, DENTIFRICE [TOM'S OF MAINE] 1 Current NDC, 3 package rows 20250101_4c535776-3f80-4eeb-bb63-2d734c3c3a6b.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 44 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 51009-920-40 51009092040 1 TUBE in 1 CARTON (51009-920-40) / 113 g in 1 TUBE 1 tube 2025-01-01 No No Current 51009-920-63 51009092063 85 g in 1 TUBE (51009-920-63) 85 g 2026-02-01 No No Current