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Probee
Probee - 76254-1001-1 - (propolis)
Drug Information of Probee
| Product NDC: | 76254-1001 |
| Proprietary Name: | Probee |
| Non Proprietary Name: | propolis |
| Active Ingredient(s): | 5 g/100g & nbsp; propolis |
| Administration Route(s): | ORAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Probee
| Product NDC: | 76254-1001 |
| Labeler Name: | Seoul Propolis |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110810 |
Package Information of Probee
| Package NDC: | 76254-1001-1 |
| Package Description: | 50 g in 1 TUBE (76254-1001-1) |
NDC Information of Probee
| NDC Code | 76254-1001-1 |
| Proprietary Name | Probee |
| Package Description | 50 g in 1 TUBE (76254-1001-1) |
| Product NDC | 76254-1001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | propolis |
| Dosage Form Name | PASTE, DENTIFRICE |
| Route Name | ORAL |
| Start Marketing Date | 20110810 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Seoul Propolis |
| Substance Name | PROPOLIS WAX |
| Strength Number | 5 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
