| Product NDC: | 50629-1005 |
| Proprietary Name: | RICHENNAPHARM |
| Non Proprietary Name: | LEVOMENTHOL |
| Active Ingredient(s): | .2; .4 mL/200mL; mL/200mL & nbsp; LEVOMENTHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 50629-1005 |
| Labeler Name: | SEWHA P&C INC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100428 |
| Package NDC: | 50629-1005-2 |
| Package Description: | 1 BOTTLE in 1 BOX (50629-1005-2) > 200 mL in 1 BOTTLE (50629-1005-1) |
| NDC Code | 50629-1005-2 |
| Proprietary Name | RICHENNAPHARM |
| Package Description | 1 BOTTLE in 1 BOX (50629-1005-2) > 200 mL in 1 BOTTLE (50629-1005-1) |
| Product NDC | 50629-1005 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | LEVOMENTHOL |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20100428 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | SEWHA P&C INC |
| Substance Name | ALPHA-TOCOPHEROL ACETATE; LEVOMENTHOL |
| Strength Number | .2; .4 |
| Strength Unit | mL/200mL; mL/200mL |
| Pharmaceutical Classes |