Home NDC 11673-237-79 Target Sensitive Whitening TP
Product NDC 11673-237
Requested package NDC 11673-237-79
11-digit product format 116730237
Labeler code 11673
Product ID 11673-237_43956b68-baa3-e170-e063-6394a90a1252
Type HUMAN OTC DRUG
Nonproprietary name Sodium fluoride
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler Target
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-02-01
Substance POTASSIUM NITRATE; SODIUM FLUORIDE
Active strength 5; .24 g/100g; g/100g
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 2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 11673-237 11673-237-79 D Discontinued by firm excluded / ndc_excluded.zip 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 11673-237 11673-237-79 D Discontinued by firm excluded / ndc_excluded.zip 557ba5c1ecfa…9c80585c8c6e…
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 Target Sensitive Whitening TP
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POTASSIUM NITRATE 5 g/100g SODIUM FLUORIDE .24 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination RU45X2JN0Z Internal UNII lookup 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 1038929 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 11673-237-79 Target Sensitive Whitening TP 113 g in 1 TUBE PASTE, DENTIFRICE 113 7 11673-237-79 Target Sensitive Whitening TP 1 in 1 CARTON PASTE, DENTIFRICE 1 7 11673-237-89 Target Sensitive Whitening TP 113 g in 1 TUBE PASTE, DENTIFRICE 113 7 11673-237-89 Target Sensitive Whitening TP 1 in 1 CARTON PASTE, DENTIFRICE 1 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11673-237 TARGET SENSITIVE WHITENING TP (SODIUM FLUORIDE) PASTE, DENTIFRICE [TARGET] 5 Current NDC, Legacy NDC, 4 package rows 20250119_ab9a129e-337b-31fe-e053-2995a90ac691.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 9 of 40 · 786 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 11673-237-79 11673023779 1 TUBE in 1 CARTON (11673-237-79) / 113 g in 1 TUBE 1 tube 2024-10-01 0000-00-00 No No Current