Colgate Triple Action is a Dental Paste, Dentifrice in the Human Otc Drug category. It is labeled and distributed by Colgate-palmolive Company. The primary component is Sodium Fluoride.
| Product ID | 35000-941_952fa194-9531-459d-b07c-49bf60a9b1b5 |
| NDC | 35000-941 |
| Product Type | Human Otc Drug |
| Proprietary Name | Colgate Triple Action |
| Generic Name | Sodium Fluoride |
| Dosage Form | Paste, Dentifrice |
| Route of Administration | DENTAL |
| Marketing Start Date | 2010-12-01 |
| Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
| Application Number | part355 |
| Labeler Name | Colgate-Palmolive Company |
| Substance Name | SODIUM FLUORIDE |
| Active Ingredient Strength | 1 mg/g |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2010-12-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part355 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-12-01 |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part355 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-12-01 |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part355 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-12-01 |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part355 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-12-01 |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part355 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-12-01 |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part355 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-12-01 |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part355 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-12-01 |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part355 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-12-01 |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part355 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-12-01 |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part355 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-12-01 |
| Ingredient | Strength |
|---|---|
| SODIUM FLUORIDE | 1.1 mg/g |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 65954-536 | Colgate Triple Action | Colgate Triple Action |
| 35000-941 | Colgate Triple Action | Colgate Triple Action |
| 0135-0234 | AQUAFRESH | sodium fluoride |
| 0126-0021 | Colgate | SODIUM FLUORIDE |
| 0126-0034 | Colgate Phos-Flur Ortho Defense Alcohol Free Anticavity Gushing Grape Fluoride | SODIUM FLUORIDE |
| 0126-0032 | Colgate Phos-Flur Ortho Defense Alcohol Free Anticavity Mint Fluoride | SODIUM FLUORIDE |
| 0041-1421 | Oral-B | Sodium Fluoride |
| 0126-0131 | Phos-Flur | Sodium Fluoride |
| 0126-0135 | Phos-Flur Ortho Defense | SODIUM FLUORIDE |
| 0126-0138 | Phos-Flur Ortho Defense | SODIUM FLUORIDE |
| 0126-0139 | Phos-Flur Ortho Defense | SODIUM FLUORIDE |
| 0126-0074 | PrevidDent 5000 Booster Plus Spearmint | Sodium Fluoride |
| 0126-0016 | PreviDent | Sodium fluoride |
| 0126-0075 | PreviDent | Sodium fluoride |
| 0126-0076 | PreviDent | Sodium fluoride |
| 0126-0179 | PreviDent | Sodium Fluoride |
| 0126-0286 | PreviDent | Sodium Fluoride |
| 0126-0287 | PreviDent | Sodium Fluoride |
| 0126-0072 | PreviDent 5000 Booster Plus Fruitastic | Sodium Fluoride |
| 0126-0033 | PreviDent Alcohol Free | Sodium Fluoride |
| 0126-0088 | PreviDent Fresh Mint | Sodium Fluoride |
| 0126-0289 | PreviDent OrthoDefense | SODIUM FLUORIDE |
| 0126-0288 | PreviDent Very Berry | Sodium Fluoride |