Home NDC 68599-9571 Fluoride
Product NDC 68599-9571
11-digit product format 685999571
Labeler code 68599
Product ID 68599-9571_4c482e45-0503-a93a-e063-6394a90aa961
Type HUMAN OTC DRUG
Nonproprietary name Fluoride Toothpaste
Dosage form PASTE
Route DENTAL
Labeler McKesson
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-03-05
Substance SODIUM MONOFLUOROPHOSPHATE
Active strength .76 g/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 Fluoride
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM MONOFLUOROPHOSPHATE .76 g/g
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 Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 68599-9571-1 Fluoride 1 g in 1 TUBE PASTE 1 1
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 68599-9571-1 68599957101 1 g in 1 TUBE (68599-9571-1) 1 g 2026-03-05 No No Current