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Crest Cavity Protection FLUORIDE ANTICAVITY
Crest Cavity Protection FLUORIDE ANTICAVITY - 67751-052-01 - (SODIUM FLUORIDE)
Drug Information of Crest Cavity Protection FLUORIDE ANTICAVITY
| Product NDC: | 67751-052 |
| Proprietary Name: | Crest Cavity Protection FLUORIDE ANTICAVITY |
| Non Proprietary Name: | SODIUM FLUORIDE |
| Active Ingredient(s): | .15 g/100g & nbsp; SODIUM FLUORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Crest Cavity Protection FLUORIDE ANTICAVITY
| Product NDC: | 67751-052 |
| Labeler Name: | Navajo Manufacturing Company Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130624 |
Package Information of Crest Cavity Protection FLUORIDE ANTICAVITY
| Package NDC: | 67751-052-01 |
| Package Description: | 1 TUBE in 1 PACKAGE (67751-052-01) > 24 g in 1 TUBE |
NDC Information of Crest Cavity Protection FLUORIDE ANTICAVITY
| NDC Code | 67751-052-01 |
| Proprietary Name | Crest Cavity Protection FLUORIDE ANTICAVITY |
| Package Description | 1 TUBE in 1 PACKAGE (67751-052-01) > 24 g in 1 TUBE |
| Product NDC | 67751-052 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM FLUORIDE |
| Dosage Form Name | PASTE, DENTIFRICE |
| Route Name | ORAL |
| Start Marketing Date | 20130624 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Navajo Manufacturing Company Inc |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | .15 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
