Home NDC 87649-0718 Anticavity mouth rinse Low-foaming Spearmint
Product NDC 87649-0718
11-digit product format 876490718
Labeler code 87649
Product ID 87649-0718_4ef669b9-deff-8965-e063-6394a90ab335
Type HUMAN OTC DRUG
Nonproprietary name 779 US Variant Anticavity mouth rinse Low-foaming Spearmint
Dosage form GEL, DENTIFRICE
Route ORAL
Labeler Dyson Technology Limited
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-07-31
Substance SODIUM FLUORIDE
Active strength .02 g/100mL
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 mouth rinse Low-foaming Spearmint
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE .02 g/100mL
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 RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 313029 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 6 of 50 · 995 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87649-0718-1 87649071801 400 mL in 1 BOTTLE (87649-0718-1) 400 ml 2026-07-31 No No Current