Home NDC 52000-108 ADVANCED WHITENING ANTI CAVITY FLUORIDE
Product NDC 52000-108
11-digit product format 520000108
Labeler code 52000
Product ID 52000-108_ede5654c-864e-44c6-904b-ca2ac4532096
Type HUMAN OTC DRUG
Nonproprietary name Sodium Monofluorophosphate
Dosage form PASTE
Route DENTAL
Labeler Universal Distribution Center LLC
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-05-18
Substance SODIUM MONOFLUOROPHOSPHATE
Active strength .76 g/100g
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 ADVANCED WHITENING ANTI CAVITY FLUORIDE
Listing expiration 2026-12-31 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.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 52000-108-01 ADVANCED WHITENING ANTI CAVITY FLUORIDE 181 g in 1 TUBE PASTE 181 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 52000-108 ADVANCED WHITENING ANTI CAVITY FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE [UNIVERSAL DISTRIBUTION CENTER LLC] 2 Current NDC, Legacy NDC, 1 package rows 20231121_8ea8a8d9-b7e4-468f-9a09-4ec634cbd80e.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 Marketing end Sample Exclude flag Status 52000-108-01 52000010801 181 g in 1 TUBE (52000-108-01) 181 g 2020-05-18 0000-00-00 No No Current