FDA.reportPublic FDA data

DOCTRUST K Tooth

Product NDC
76670-0014
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

Additional Listing Data#

Finished product
Yes
Brand name base
DOCTRUST K Tooth
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SILICON DIOXIDE16 g/100g
SODIUM MONOFLUOROPHOSPHATE.74 g/100g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiETJ7Z6XBU4, C810JCZ56Q

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76670-0014-1DOCTRUST K Tooth60 g in 1 TUBEGEL, DENTIFRICE603
76670-0014-2DOCTRUST K Tooth1 in 1 CARTONGEL, DENTIFRICE13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76670-0014DOCTRUST K TOOTH (SILICON DIOXIDE, SODIUM MONOFLUOROPHOSPHATE) GEL, DENTIFRICE [DOCSMEDI CO., LTD.]3Current NDC, Legacy NDC, 2 package rows20250123_a02f8865-e7be-4ef4-b09c-dad846639764.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
76670-0014-17667000140160 g in 1 TUBE60 gHistorical
76670-0014-2766700014021 TUBE in 1 CARTON (76670-0014-2) / 60 g in 1 TUBE (76670-0014-1) 1 tube2022-12-010000-00-00NoNoCurrent