Home NDC 82913-004 AutoBrush Mint
Product NDC 82913-004
11-digit product format 829130004
Labeler code 82913
Product ID 82913-004_47433424-5a70-96b0-e063-6394a90a269f
Type HUMAN OTC DRUG
Nonproprietary name Sodium Fluoride
Dosage form LIQUID
Route ORAL
Labeler Lander Enterprises, LLC
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-12-01
Substance SODIUM FLUORIDE
Active strength .24 g/100mL
NDC exclude flag No
Listing certified through 2026-12-31
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 2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 82913-004 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 82913-004 82913-004-01 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…
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 AutoBrush Mint
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE .24 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 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 82913-004-01 AutoBrush Mint 1 in 1 CARTON LIQUID 1 5 82913-004-01 AutoBrush Mint 50 mL in 1 BOTTLE, PLASTIC LIQUID 50 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 82913-004 AUTOBRUSH MINT (SODIUM FLUORIDE) LIQUID [LANDER ENTERPRISES, LLC] 4 Current NDC, Legacy NDC, 2 package rows 20250223_6bcd35f5-18ea-4fc8-84cd-06db73f38a1e.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 32 of 40 · 786 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 82913-004-01 82913000401 1 BOTTLE, PLASTIC in 1 CARTON (82913-004-01) / 50 mL in 1 BOTTLE, PLASTIC 2022-12-01 0000-00-00 No No Current