Home NDC 72705-503-01 Frida Fluoride Bubble Mint
Product NDC 72705-503
Requested package NDC 72705-503-01
11-digit product format 727050503
Labeler code 72705
Product ID 72705-503_5127a8e8-3229-18ff-e063-6394a90ae5b5
Type HUMAN OTC DRUG
Nonproprietary name Sodium fluoride
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler Fridababy, LLC
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-01
Substance SODIUM FLUORIDE
Active strength 2.2 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 Frida Fluoride Bubble Mint
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE 2.2 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 245598 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 38 of 49 · 974 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 72705-503-01 72705050301 1 TUBE in 1 CARTON (72705-503-01) / 113 g in 1 TUBE 1 tube 2026-08-01 No No Current