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Colgate
Colgate - 0126-0021-03 - (SODIUM FLUORIDE)
Drug Information of Colgate
| Product NDC: | 0126-0021 |
| Proprietary Name: | Colgate |
| Non Proprietary Name: | SODIUM FLUORIDE |
| Active Ingredient(s): | 2.1 mg/10mL & nbsp; SODIUM FLUORIDE |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | RINSE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Colgate
| Product NDC: | 0126-0021 |
| Labeler Name: | Colgate Oral Pharmaceuticals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110114 |
Package Information of Colgate
| Package NDC: | 0126-0021-03 |
| Package Description: | 59 mL in 1 BOTTLE (0126-0021-03) |
NDC Information of Colgate
| NDC Code | 0126-0021-03 |
| Proprietary Name | Colgate |
| Package Description | 59 mL in 1 BOTTLE (0126-0021-03) |
| Product NDC | 0126-0021 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM FLUORIDE |
| Dosage Form Name | RINSE |
| Route Name | DENTAL |
| Start Marketing Date | 20110114 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Colgate Oral Pharmaceuticals, Inc. |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | 2.1 |
| Strength Unit | mg/10mL |
| Pharmaceutical Classes |
