Product NDC: | 35000-002 |
Proprietary Name: | Colgate |
Non Proprietary Name: | Silicon Dioxide, Sodium Fluoride, and Triclosan |
Active Ingredient(s): | 50; 2.4; 3 mg/g; mg/g; mg/g & nbsp; Silicon Dioxide, Sodium Fluoride, and Triclosan |
Administration Route(s): | DENTAL |
Dosage Form(s): | GEL, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 35000-002 |
Labeler Name: | Colgate-Palmolive Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | NDA020231 |
Marketing Category: | NDA |
Start Marketing Date: | 20100920 |
Package NDC: | 35000-002-60 |
Package Description: | 1 TUBE in 1 CARTON (35000-002-60) > 170 g in 1 TUBE |
NDC Code | 35000-002-60 |
Proprietary Name | Colgate |
Package Description | 1 TUBE in 1 CARTON (35000-002-60) > 170 g in 1 TUBE |
Product NDC | 35000-002 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Silicon Dioxide, Sodium Fluoride, and Triclosan |
Dosage Form Name | GEL, DENTIFRICE |
Route Name | DENTAL |
Start Marketing Date | 20100920 |
Marketing Category Name | NDA |
Labeler Name | Colgate-Palmolive Company |
Substance Name | SILICON DIOXIDE; SODIUM FLUORIDE; TRICLOSAN |
Strength Number | 50; 2.4; 3 |
Strength Unit | mg/g; mg/g; mg/g |
Pharmaceutical Classes |