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Morning Fresh
Morning Fresh - 67777-172-01 - (Sodium Monofluorophosphate)
Drug Information of Morning Fresh
| Product NDC: | 67777-172 |
| Proprietary Name: | Morning Fresh |
| Non Proprietary Name: | Sodium Monofluorophosphate |
| Active Ingredient(s): | 1 mg/g & nbsp; Sodium Monofluorophosphate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | PASTE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Morning Fresh
| Product NDC: | 67777-172 |
| Labeler Name: | Dynarex Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130405 |
Package Information of Morning Fresh
| Package NDC: | 67777-172-01 |
| Package Description: | 43 g in 1 TUBE (67777-172-01) |
NDC Information of Morning Fresh
| NDC Code | 67777-172-01 |
| Proprietary Name | Morning Fresh |
| Package Description | 43 g in 1 TUBE (67777-172-01) |
| Product NDC | 67777-172 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium Monofluorophosphate |
| Dosage Form Name | PASTE |
| Route Name | ORAL |
| Start Marketing Date | 20130405 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Dynarex Corporation |
| Substance Name | SODIUM MONOFLUOROPHOSPHATE |
| Strength Number | 1 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
