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PROPOLIS
PROPOLIS - 52257-1208-1 - (SODIUM MONOFLUOROPHOSPHATE)
Drug Information of PROPOLIS
| Product NDC: | 52257-1208 |
| Proprietary Name: | PROPOLIS |
| Non Proprietary Name: | SODIUM MONOFLUOROPHOSPHATE |
| Active Ingredient(s): | .05; .08 g/50g; g/50g & nbsp; SODIUM MONOFLUOROPHOSPHATE |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PROPOLIS
| Product NDC: | 52257-1208 |
| Labeler Name: | ATOMY CO., LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100525 |
Package Information of PROPOLIS
| Package NDC: | 52257-1208-1 |
| Package Description: | 50 g in 1 CARTON (52257-1208-1) |
NDC Information of PROPOLIS
| NDC Code | 52257-1208-1 |
| Proprietary Name | PROPOLIS |
| Package Description | 50 g in 1 CARTON (52257-1208-1) |
| Product NDC | 52257-1208 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM MONOFLUOROPHOSPHATE |
| Dosage Form Name | PASTE, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20100525 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | ATOMY CO., LTD. |
| Substance Name | SODIUM FLUORIDE; SODIUM MONOFLUOROPHOSPHATE |
| Strength Number | .05; .08 |
| Strength Unit | g/50g; g/50g |
| Pharmaceutical Classes |
