Home NDC 72288-213 Anticavity Fluoride Rinse
Product NDC 72288-213
11-digit product format 722880213
Labeler code 72288
Product ID 72288-213_5ca1e1be-f034-6a8e-e063-6394a90ab5b2
Type HUMAN OTC DRUG
Nonproprietary name Sodium Fluoride
Dosage form MOUTHWASH
Route ORAL
Labeler Amazon.com Services LLC
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-04-24
Substance SODIUM FLUORIDE
Active strength .2 mg/mL
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 Fluoride Rinse
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE .2 mg/mL
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72288-213-44 Anticavity Fluoride Rinse 532 mL in 1 BOTTLE, PLASTIC MOUTHWASH 532 19
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72288-213 ANTICAVITY FLUORIDE RINSE (SODIUM FLUORIDE) MOUTHWASH [AMAZON.COM SERVICES LLC] 17 Current NDC, Legacy NDC, 1 package rows 20250426_f275755f-7879-4ca1-ae03-fa709e88cdad.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 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 Marketing end Sample Exclude flag Status 72288-213-44 72288021344 532 mL in 1 BOTTLE, PLASTIC (72288-213-44) 532 ml 2018-04-24 0000-00-00 No No Current