Product NDC: | 41163-822 |
Proprietary Name: | Witch Hazel |
Non Proprietary Name: | Witch Hazel |
Active Ingredient(s): | .86 kg/100L & nbsp; Witch Hazel |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 41163-822 |
Labeler Name: | Supervalu, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part347 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090529 |
Package NDC: | 41163-822-43 |
Package Description: | .473 L in 1 BOTTLE, PLASTIC (41163-822-43) |
NDC Code | 41163-822-43 |
Proprietary Name | Witch Hazel |
Package Description | .473 L in 1 BOTTLE, PLASTIC (41163-822-43) |
Product NDC | 41163-822 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Witch Hazel |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20090529 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Supervalu, Inc |
Substance Name | WITCH HAZEL |
Strength Number | .86 |
Strength Unit | kg/100L |
Pharmaceutical Classes |