Product NDC: | 35000-027 |
Proprietary Name: | Colgate Total Zx Pro-Shield Plus Sensitive |
Non Proprietary Name: | Sodium Monofluorophosphate, Zinc Citrate Trihydrate, and Potassium Nitrate |
Active Ingredient(s): | 2.4; .55; .96 mg/g; mg/g; mg/g & nbsp; Sodium Monofluorophosphate, Zinc Citrate Trihydrate, and Potassium Nitrate |
Administration Route(s): | DENTAL |
Dosage Form(s): | PASTE, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 35000-027 |
Labeler Name: | Colgate-Palmolive |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | NDA020231 |
Marketing Category: | NDA |
Start Marketing Date: | 20130201 |
Package NDC: | 35000-027-66 |
Package Description: | 1 TUBE in 1 CARTON (35000-027-66) > 164 g in 1 TUBE |
NDC Code | 35000-027-66 |
Proprietary Name | Colgate Total Zx Pro-Shield Plus Sensitive |
Package Description | 1 TUBE in 1 CARTON (35000-027-66) > 164 g in 1 TUBE |
Product NDC | 35000-027 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Sodium Monofluorophosphate, Zinc Citrate Trihydrate, and Potassium Nitrate |
Dosage Form Name | PASTE, DENTIFRICE |
Route Name | DENTAL |
Start Marketing Date | 20130201 |
Marketing Category Name | NDA |
Labeler Name | Colgate-Palmolive |
Substance Name | POTASSIUM NITRATE; SODIUM MONOFLUOROPHOSPHATE; ZINC CITRATE TRIHYDRATE |
Strength Number | 2.4; .55; .96 |
Strength Unit | mg/g; mg/g; mg/g |
Pharmaceutical Classes |