Home NDC 53247-130 Maximum Security
Product NDC 53247-130
11-digit product format 532470130
Labeler code 53247
Product ID 53247-130_3d24a0e7-3e0d-495b-a3ba-1ca883da5ae5
Type HUMAN OTC DRUG
Nonproprietary name Sodium Fluoride
Dosage form GEL, DENTIFRICE
Route DENTAL
Labeler Bob Barker Company Inc.
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2008-01-01
Substance SODIUM FLUORIDE
Active strength 2.2 mg/g
NDC exclude flag No
Listing certified through 2026-12-31
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 Maximum Security
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE 2.2 mg/g
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 245598 Internal RxNorm 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 53247-130-01 Maximum Security 4.3 g in 1 PACKET GEL, DENTIFRICE 4.3 2 53247-130-02 Maximum Security 17 g in 1 TUBE GEL, DENTIFRICE 17 2 53247-130-03 Maximum Security 24 g in 1 TUBE GEL, DENTIFRICE 24 2 53247-130-04 Maximum Security 43 g in 1 TUBE GEL, DENTIFRICE 43 2 53247-130-05 Maximum Security 130 g in 1 TUBE GEL, DENTIFRICE 130 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 53247-130 MAXIMUM SECURITY (SODIUM FLUORIDE) GEL, DENTIFRICE [BOB BARKER COMPANY INC.] 2 Current NDC, 5 package rows 20240306_e29f30ec-72ea-4944-a2c2-b1696d31b639.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 Sample Exclude flag Status 53247-130-01 53247013001 4.3 g in 1 PACKET (53247-130-01) 4.3 g 2008-01-01 No No Current 53247-130-02 53247013002 17 g in 1 TUBE (53247-130-02) 17 g 2008-01-01 No No Current 53247-130-03 53247013003 24 g in 1 TUBE (53247-130-03) 24 g 2008-01-01 No No Current 53247-130-04 53247013004 43 g in 1 TUBE (53247-130-04) 43 g 2008-01-01 No No Current 53247-130-05 53247013005 130 g in 1 TUBE (53247-130-05) 130 g 2008-01-01 No No Current