Home NDC 79940-012 Colgate Anticavity
Product NDC 79940-012
11-digit product format 799400012
Labeler code 79940
Product ID 79940-012_4a69d2a6-df7f-78ef-e063-6294a90ade39
Type HUMAN OTC DRUG
Nonproprietary name SODIUM MONOFLUOROPHOSPHATE
Dosage form KIT
Labeler FORMIA LIMITED
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-01-01
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 Colgate Anticavity
Listing expiration 2027-12-31 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 79940-012-00 Colgate Anticavity 1 in 1 KIT KIT 1 2
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.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 79940-012-00 79940001200 1 KIT in 1 KIT (79940-012-00) * 5 g in 1 TUBE (42555-060-94) 1 kit 2026-01-01 No No Current