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Go Smile
Go Smile - 44873-003-01 - (SODIUM MONOFLUOROPHOSPHATE)
Drug Information of Go Smile
| Product NDC: | 44873-003 |
| Proprietary Name: | Go Smile |
| Non Proprietary Name: | SODIUM MONOFLUOROPHOSPHATE |
| Active Ingredient(s): | .76 g/100g & nbsp; SODIUM MONOFLUOROPHOSPHATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Go Smile
| Product NDC: | 44873-003 |
| Labeler Name: | Go Smile, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110505 |
Package Information of Go Smile
| Package NDC: | 44873-003-01 |
| Package Description: | 28 g in 1 TUBE (44873-003-01) |
NDC Information of Go Smile
| NDC Code | 44873-003-01 |
| Proprietary Name | Go Smile |
| Package Description | 28 g in 1 TUBE (44873-003-01) |
| Product NDC | 44873-003 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM MONOFLUOROPHOSPHATE |
| Dosage Form Name | PASTE, DENTIFRICE |
| Route Name | ORAL |
| Start Marketing Date | 20110505 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Go Smile, Inc. |
| Substance Name | SODIUM MONOFLUOROPHOSPHATE |
| Strength Number | .76 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
