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Country Gent
Country Gent - 66894-0000-1 - (SODIUM FLUORIDE)
Drug Information of Country Gent
| Product NDC: | 66894-0000 |
| Proprietary Name: | Country Gent |
| Non Proprietary Name: | SODIUM FLUORIDE |
| Active Ingredient(s): | 1.88 mg/g & nbsp; SODIUM FLUORIDE |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | POWDER, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Country Gent
| Product NDC: | 66894-0000 |
| Labeler Name: | Heavenly Harvest, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120101 |
Package Information of Country Gent
| Package NDC: | 66894-0000-1 |
| Package Description: | 113 g in 1 BOTTLE (66894-0000-1) |
NDC Information of Country Gent
| NDC Code | 66894-0000-1 |
| Proprietary Name | Country Gent |
| Package Description | 113 g in 1 BOTTLE (66894-0000-1) |
| Product NDC | 66894-0000 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM FLUORIDE |
| Dosage Form Name | POWDER, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20120101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Heavenly Harvest, Inc. |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | 1.88 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
