Home NDC 76670-0010 DOCTRUST DOUBLEX Tooth
Product NDC 76670-0010
11-digit product format 766700010
Labeler code 76670
Product ID 76670-0010_2c47f6e9-359f-4f4e-e063-6394a90a6353
Type HUMAN OTC DRUG
Nonproprietary name Sodium fluoride
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler DOCSMEDI Co., Ltd.
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-10-01
Substance SODIUM FLUORIDE
Active strength .22 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 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 76670-0010-2 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 76670-0010-2 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 DOUBLEX Tooth
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE .22 g/100g
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 76670-0010-1 DOCTRUST DOUBLEX Tooth 100 g in 1 TUBE PASTE, DENTIFRICE 100 5 76670-0010-2 DOCTRUST DOUBLEX Tooth 1 in 1 CARTON PASTE, DENTIFRICE 1 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 76670-0010 DOCTRUST DOUBLEX TOOTH (SODIUM FLUORIDE) PASTE, DENTIFRICE [DOCSMEDI CO., LTD.] 5 Current NDC, Legacy NDC, 2 package rows 20250123_aaf08481-a2ff-48f6-8611-73a469efe1db.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 35 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 76670-0010-1 76670001001 100 g in 1 TUBE 100 g Historical 76670-0010-2 76670001002 1 TUBE in 1 CARTON (76670-0010-2) / 100 g in 1 TUBE (76670-0010-1) 1 tube 2021-10-01 0000-00-00 No No Current