Home NDC 72476-204 Anticavity Rinse
Product NDC 72476-204
11-digit product format 724760204
Labeler code 72476
Product ID 72476-204_4a2a74ea-7002-a5dc-e063-6294a90ab5e3
Type HUMAN OTC DRUG
Nonproprietary name Sodium Fluoride
Dosage form MOUTHWASH
Route ORAL
Labeler Retail Business Services, LLC
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2010-03-10
Substance SODIUM FLUORIDE
Active strength .2 mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 72476-204 72476-204-77 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 72476-204 72476-204-77 D Discontinued by firm excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…
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 Rinse
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE .2 mg/mL
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 240698 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72476-204-44 Anticavity Rinse 532 mL in 1 BOTTLE, PLASTIC MOUTHWASH 532 8 72476-204-77 Anticavity Rinse 500 mL in 1 BOTTLE, PLASTIC MOUTHWASH 500 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72476-204 ANTICAVITY RINSE (SODIUM FLUORIDE) MOUTHWASH [RETAIL BUSINESS SERVICES, LLC] 7 Current NDC, Legacy NDC, 2 package rows 20250523_77c066cf-f064-45d3-9732-4433165ba9ef.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 22 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 72476-204-44 72476020444 532 mL in 1 BOTTLE, PLASTIC (72476-204-44) 532 ml 2010-03-10 0000-00-00 No No Current 72476-204-77 72476020477 500 mL in 1 BOTTLE, PLASTIC (72476-204-77) 500 ml 2010-03-10 0000-00-00 No No Current