| Product NDC: | 76254-5001 |
| Proprietary Name: | Seoul Propolia |
| Non Proprietary Name: | propolis |
| Active Ingredient(s): | .99 mL/mL & nbsp; propolis |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 76254-5001 |
| Labeler Name: | Seoul Propolis |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110816 |
| Package NDC: | 76254-5001-1 |
| Package Description: | 30 mL in 1 BOTTLE, GLASS (76254-5001-1) |
| NDC Code | 76254-5001-1 |
| Proprietary Name | Seoul Propolia |
| Package Description | 30 mL in 1 BOTTLE, GLASS (76254-5001-1) |
| Product NDC | 76254-5001 |
| 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 | .99 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |