Home NDC 66975-782 Prosys
Product NDC 66975-782
11-digit product format 669750782
Labeler code 66975
Product ID 66975-782_500d9ff5-0091-fc40-e063-6394a90a8810
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name 1.1% Sodium Fluoride
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler Benco Dental
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2026-02-01
Substance SODIUM FLUORIDE
Active strength .11 g/100g
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Prosys
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE .11 g/100g
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 392038 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 66975-782-01 Prosys 113 g in 1 TUBE PASTE, DENTIFRICE 113 2
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 1 of 1 · 1 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 66975-782-01 66975078201 113 g in 1 TUBE (66975-782-01) 113 g 2026-02-01 No No Current