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 |