Home NDC 87649-0907 Anticavity and sensitive peppermint
Product NDC 87649-0907
11-digit product format 876490907
Labeler code 87649
Product ID 87649-0907_5574805e-4cfe-843a-e063-6294a90a47d7
Type HUMAN OTC DRUG
Nonproprietary name 907 US variant Anticavity and sensitive toothpaste non foaming peppermint
Dosage form PASTE, DENTIFRICE
Route ORAL
Labeler Dyson Technology Limited
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-06-10
Substance SODIUM FLUORIDE; POTASSIUM NITRATE
Active strength .243; 5 g/100g; g/100g
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 and sensitive peppermint
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE .243 g/100g POTASSIUM NITRATE 5 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 8ZYQ1474W7 Internal UNII lookup RU45X2JN0Z Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1038800 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 9 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 87649-0907-1 87649090701 94.5 g in 1 TUBE (87649-0907-1) 94.5 g 2026-06-10 No No Current