Home NDC 73656-034 Optimax Purple Anticavity Fluoride
Product NDC 73656-034
11-digit product format 736560034
Labeler code 73656
Product ID 73656-034_3dd7ebc9-b4c9-92b0-e063-6394a90a068c
Type HUMAN OTC DRUG
Nonproprietary name SODIUM MONOFLUOROPHOSPHATE
Dosage form KIT
Labeler WHITE GLO USA INC
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-03-31
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 Purple Anticavity Fluoride
Listing expiration 2026-12-31 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 73656-034-00 Optimax Purple Anticavity Fluoride 1 in 1 KIT KIT 1 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 39 of 50 · 995 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 73656-034-00 73656003400 1 KIT in 1 KIT (73656-034-00) * 2 TUBE in 1 BOX (73656-035-00) / 150 g in 1 TUBE 1 kit 2025-03-31 No No Current