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Jason Sea Fresh Anticavity Strengthening Deep Sea Spearmint
Jason Sea Fresh Anticavity Strengthening Deep Sea Spearmint - 61995-0104-6 - (Sodium Monofluorophosphate)
Drug Information of Jason Sea Fresh Anticavity Strengthening Deep Sea Spearmint
| Product NDC: | 61995-0104 |
| Proprietary Name: | Jason Sea Fresh Anticavity Strengthening Deep Sea Spearmint |
| Non Proprietary Name: | Sodium Monofluorophosphate |
| Active Ingredient(s): | .76 g/100g & nbsp; Sodium Monofluorophosphate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Jason Sea Fresh Anticavity Strengthening Deep Sea Spearmint
| Product NDC: | 61995-0104 |
| Labeler Name: | The Hain Celestial Group, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110920 |
Package Information of Jason Sea Fresh Anticavity Strengthening Deep Sea Spearmint
| Package NDC: | 61995-0104-6 |
| Package Description: | 1 TUBE in 1 CARTON (61995-0104-6) > 170 g in 1 TUBE |
NDC Information of Jason Sea Fresh Anticavity Strengthening Deep Sea Spearmint
| NDC Code | 61995-0104-6 |
| Proprietary Name | Jason Sea Fresh Anticavity Strengthening Deep Sea Spearmint |
| Package Description | 1 TUBE in 1 CARTON (61995-0104-6) > 170 g in 1 TUBE |
| Product NDC | 61995-0104 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium Monofluorophosphate |
| Dosage Form Name | GEL |
| Route Name | ORAL |
| Start Marketing Date | 20110920 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | The Hain Celestial Group, Inc. |
| Substance Name | SODIUM MONOFLUOROPHOSPHATE |
| Strength Number | .76 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
