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E ENZYME
E ENZYME - 76414-010-01 - (SODIUM MONOFLUOROPHOSPHATE)
Drug Information of E ENZYME
| Product NDC: | 76414-010 |
| Proprietary Name: | E ENZYME |
| Non Proprietary Name: | SODIUM MONOFLUOROPHOSPHATE |
| Active Ingredient(s): | 1.2 g/200g & nbsp; SODIUM MONOFLUOROPHOSPHATE |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of E ENZYME
| Product NDC: | 76414-010 |
| Labeler Name: | SAMJOKO SKYBLUE CO., LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110301 |
Package Information of E ENZYME
| Package NDC: | 76414-010-01 |
| Package Description: | 200 g in 1 CARTON (76414-010-01) |
NDC Information of E ENZYME
| NDC Code | 76414-010-01 |
| Proprietary Name | E ENZYME |
| Package Description | 200 g in 1 CARTON (76414-010-01) |
| Product NDC | 76414-010 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM MONOFLUOROPHOSPHATE |
| Dosage Form Name | PASTE, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20110301 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | SAMJOKO SKYBLUE CO., LTD. |
| Substance Name | SODIUM MONOFLUOROPHOSPHATE |
| Strength Number | 1.2 |
| Strength Unit | g/200g |
| Pharmaceutical Classes |
