Product NDC: | 51346-199 |
Proprietary Name: | SNAYTOX HYDROGEL LIP |
Non Proprietary Name: | Witch Hazel |
Active Ingredient(s): | .1 g/10g & nbsp; Witch Hazel |
Administration Route(s): | TOPICAL |
Dosage Form(s): | PATCH |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51346-199 |
Labeler Name: | NATURE REPUBLIC CO., LTD. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part347 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120701 |
Package NDC: | 51346-199-01 |
Package Description: | 10 g in 1 CARTON (51346-199-01) |
NDC Code | 51346-199-01 |
Proprietary Name | SNAYTOX HYDROGEL LIP |
Package Description | 10 g in 1 CARTON (51346-199-01) |
Product NDC | 51346-199 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Witch Hazel |
Dosage Form Name | PATCH |
Route Name | TOPICAL |
Start Marketing Date | 20120701 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | NATURE REPUBLIC CO., LTD. |
Substance Name | WITCH HAZEL |
Strength Number | .1 |
Strength Unit | g/10g |
Pharmaceutical Classes |