Product NDC: | 49742-1001 |
Proprietary Name: | Skin-ion |
Non Proprietary Name: | ARBUTIN, ADENOSINE, GLYCERIN |
Active Ingredient(s): | .016; .8; .8 mL/40mL; mL/40mL; mL/40mL & nbsp; ARBUTIN, ADENOSINE, GLYCERIN |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49742-1001 |
Labeler Name: | WAKO Korea Corp |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part347 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100101 |
Package NDC: | 49742-1001-1 |
Package Description: | 40 mL in 1 CARTON (49742-1001-1) |
NDC Code | 49742-1001-1 |
Proprietary Name | Skin-ion |
Package Description | 40 mL in 1 CARTON (49742-1001-1) |
Product NDC | 49742-1001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ARBUTIN, ADENOSINE, GLYCERIN |
Dosage Form Name | SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 20100101 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | WAKO Korea Corp |
Substance Name | ADENOSINE; ARBUTIN; GLYCERIN |
Strength Number | .016; .8; .8 |
Strength Unit | mL/40mL; mL/40mL; mL/40mL |
Pharmaceutical Classes |