Home NDC 55319-193 Anticavity Fluoride
Product NDC 55319-193
11-digit product format 553190193
Labeler code 55319
Product ID 55319-193_c3f30f5b-9b5e-4515-bdff-80c5c37ef25d
Type HUMAN OTC DRUG
Nonproprietary name Sodium Fluoride and Acidulated Phosphate
Dosage form LIQUID
Route ORAL
Labeler Family Dollar (FAMILY WELLNESS)
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-06-02
Substance SODIUM FLUORIDE
Active strength .1 mg/mL
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 Anticavity Fluoride
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE .1 mg/mL
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 55319-193-01 Anticavity Fluoride 1000 mL in 1 BOTTLE, PLASTIC LIQUID 1000 3
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 14 of 40 · 786 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 55319-193-01 55319019301 1000 mL in 1 BOTTLE, PLASTIC (55319-193-01) 1000 ml 2025-06-02 No No Current