Home NDC 11291-243 Dr Tichenors With Extra Whitening and Tartar Control
Product NDC 11291-243
11-digit product format 112910243
Labeler code 11291
Product ID 11291-243_436b89b3-2823-085f-e063-6294a90a40aa
Type HUMAN OTC DRUG
Nonproprietary name Sodium Fluoride
Dosage form PASTE, DENTIFRICE
Route ORAL
Labeler Dr. G. H. Tichenor's Antiseptic Company
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2012-10-24
Substance SODIUM FLUORIDE
Active strength 2.43 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 Dr Tichenors With Extra Whitening and Tartar Control
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE 2.43 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 891775 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 11291-243-01 Dr Tichenors With Extra Whitening and Tartar Control 181 g in 1 TUBE PASTE, DENTIFRICE 181 8 11291-243-02 Dr Tichenors With Extra Whitening and Tartar Control 1 in 1 CARTON PASTE, DENTIFRICE 1 8
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11291-243 DR TICHENORS WITH EXTRA WHITENING AND TARTAR CONTROL (SODIUM FLUORIDE) PASTE, DENTIFRICE [DR. G. H. TICHENOR'S ANTISEPTIC COMPANY] 7 Current NDC, Legacy NDC, 2 package rows 20250112_bce596e8-07eb-4e56-9007-9d283e14372d.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 39 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 11291-243-01 11291024301 181 g in 1 TUBE 181 g Historical 11291-243-02 11291024302 1 TUBE in 1 CARTON (11291-243-02) / 181 g in 1 TUBE (11291-243-01) 1 tube 2012-10-24 0000-00-00 No No Current