| Product NDC: | 76254-4001 | 
| Proprietary Name: | Probee water soluble propolis | 
| Non Proprietary Name: | propolis | 
| Active Ingredient(s): | .329 mL/mL & nbsp; propolis | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | LIQUID | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 76254-4001 | 
| Labeler Name: | Seoul Propolis | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER | 
| Start Marketing Date: | 20110816 | 
| Package NDC: | 76254-4001-1 | 
| Package Description: | 30 mL in 1 BOTTLE, GLASS (76254-4001-1) | 
| NDC Code | 76254-4001-1 | 
| Proprietary Name | Probee water soluble propolis | 
| Package Description | 30 mL in 1 BOTTLE, GLASS (76254-4001-1) | 
| Product NDC | 76254-4001 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | propolis | 
| Dosage Form Name | LIQUID | 
| Route Name | ORAL | 
| Start Marketing Date | 20110816 | 
| Marketing Category Name | UNAPPROVED DRUG OTHER | 
| Labeler Name | Seoul Propolis | 
| Substance Name | PROPOLIS WAX | 
| Strength Number | .329 | 
| Strength Unit | mL/mL | 
| Pharmaceutical Classes |