Home NDC 73656-032 Optimax Anticavity Fluoride Watermelon
Product NDC 73656-032
11-digit product format 736560032
Labeler code 73656
Product ID 73656-032_34f34256-f481-6fe6-e063-6394a90af80b
Type HUMAN OTC DRUG
Nonproprietary name SODIUM MONOFLUOROPHOSPHATE
Dosage form PASTE
Route DENTAL
Labeler WHITE GLO USA INC
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-04-04
Substance SODIUM MONOFLUOROPHOSPHATE
Active strength 7.6 mg/g
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 Optimax Anticavity Fluoride Watermelon
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM MONOFLUOROPHOSPHATE 7.6 mg/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 Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 73656-032-00 Optimax Anticavity Fluoride Watermelon 1 in 1 BOX PASTE 1 1 73656-032-00 Optimax Anticavity Fluoride Watermelon 80 g in 1 TUBE PASTE 80 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73656-032 OPTIMAX ANTICAVITY FLUORIDE WATERMELON (SODIUM MONOFLUOROPHOSPHATE) PASTE [WHITE GLO USA INC] 1 Current NDC, 2 package rows 20250514_b506df13-649f-4615-bc25-6ae08bd56b18.zip
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 6 of 51 · 1,013 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 73656-032-00 73656003200 1 TUBE in 1 BOX (73656-032-00) / 80 g in 1 TUBE 1 tube 2025-04-04 No No Current