Home NDC 76670-0014-2 DOCTRUST K Tooth
Product NDC 76670-0014
Requested package NDC 76670-0014-2
11-digit product format 766700014
Labeler code 76670
Product ID 76670-0014_2c484532-89d7-c8d3-e063-6294a90a793d
Type HUMAN OTC DRUG
Nonproprietary name Silicon dioxide, Sodium monofluorophosphate
Dosage form GEL, DENTIFRICE
Route DENTAL
Labeler DOCSMEDI Co., Ltd.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2022-12-01
Substance SILICON DIOXIDE; SODIUM MONOFLUOROPHOSPHATE
Active strength 16; .74 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 2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 76670-0014 76670-0014-2 U Excluded because listing certification expired excluded / ndc_excluded.zip ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 76670-0014 76670-0014-2 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 DOCTRUST K Tooth
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SILICON DIOXIDE 16 g/100g SODIUM MONOFLUOROPHOSPHATE .74 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination ETJ7Z6XBU4 Internal UNII lookup C810JCZ56Q 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 76670-0014-1 DOCTRUST K Tooth 60 g in 1 TUBE GEL, DENTIFRICE 60 3 76670-0014-2 DOCTRUST K Tooth 1 in 1 CARTON GEL, DENTIFRICE 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 76670-0014 DOCTRUST K TOOTH (SILICON DIOXIDE, SODIUM MONOFLUOROPHOSPHATE) GEL, DENTIFRICE [DOCSMEDI CO., LTD.] 3 Current NDC, Legacy NDC, 2 package rows 20250123_a02f8865-e7be-4ef4-b09c-dad846639764.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 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 76670-0014-2 76670001402 1 TUBE in 1 CARTON (76670-0014-2) / 60 g in 1 TUBE (76670-0014-1) 1 tube 2022-12-01 0000-00-00 No No Current