| Product NDC: | 54948-100 |
| Proprietary Name: | BAEKNYONDONGAN TREATMENT |
| Non Proprietary Name: | WITCH HAZEL |
| Active Ingredient(s): | .55 mL/550mL & nbsp; WITCH HAZEL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 54948-100 |
| Labeler Name: | MIX & MATCH CO., LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110803 |
| Package NDC: | 54948-100-01 |
| Package Description: | 550 mL in 1 BOTTLE (54948-100-01) |
| NDC Code | 54948-100-01 |
| Proprietary Name | BAEKNYONDONGAN TREATMENT |
| Package Description | 550 mL in 1 BOTTLE (54948-100-01) |
| Product NDC | 54948-100 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | WITCH HAZEL |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110803 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | MIX & MATCH CO., LTD. |
| Substance Name | WITCH HAZEL |
| Strength Number | .55 |
| Strength Unit | mL/550mL |
| Pharmaceutical Classes |