Home NDC 82756-221 Tidalove
Product NDC 82756-221
11-digit product format 827560221
Labeler code 82756
Product ID 82756-221_40946943-21d0-b114-e063-6394a90aed3f
Type HUMAN OTC DRUG
Nonproprietary name Yuzu Mint Toothpaste Tablets
Dosage form TABLET, CHEWABLE
Route DENTAL
Labeler Paranmare LLC
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-10-01
Substance SODIUM FLUORIDE
Active strength .32 mg/1
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 Tidalove
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE .32 mg/1
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 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 82756-221-62 Tidalove 62 in 1 POUCH TABLET, CHEWABLE 62 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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 82756-221-62 82756022162 62 TABLET, CHEWABLE in 1 POUCH (82756-221-62) 2025-10-01 No No Current