Product NDC: | 50964-070 |
Proprietary Name: | HAMSOA YUYU DERMA119 |
Non Proprietary Name: | WITCH HAZEL |
Active Ingredient(s): | .08 g/80g & nbsp; WITCH HAZEL |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50964-070 |
Labeler Name: | HAMSOA PHARMACEUTICAL CO., LTD. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part347 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120301 |
Package NDC: | 50964-070-01 |
Package Description: | 80 g in 1 CARTON (50964-070-01) |
NDC Code | 50964-070-01 |
Proprietary Name | HAMSOA YUYU DERMA119 |
Package Description | 80 g in 1 CARTON (50964-070-01) |
Product NDC | 50964-070 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | WITCH HAZEL |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20120301 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | HAMSOA PHARMACEUTICAL CO., LTD. |
Substance Name | WITCH HAZEL |
Strength Number | .08 |
Strength Unit | g/80g |
Pharmaceutical Classes |