Product NDC: | 53077-8001 |
Proprietary Name: | Dr. Dream Urban Protective Advanced BB |
Non Proprietary Name: | WITCH HAZEL |
Active Ingredient(s): | .1 mg/100mL & nbsp; WITCH HAZEL |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 53077-8001 |
Labeler Name: | Dr. Dream Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part347 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120925 |
Package NDC: | 53077-8001-1 |
Package Description: | 30 mL in 1 TUBE (53077-8001-1) |
NDC Code | 53077-8001-1 |
Proprietary Name | Dr. Dream Urban Protective Advanced BB |
Package Description | 30 mL in 1 TUBE (53077-8001-1) |
Product NDC | 53077-8001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | WITCH HAZEL |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20120925 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Dr. Dream Inc |
Substance Name | WITCH HAZEL |
Strength Number | .1 |
Strength Unit | mg/100mL |
Pharmaceutical Classes |