Product NDC: | 62032-513 |
Proprietary Name: | NU-DERM SYSTEM NORMAL-OILY |
Non Proprietary Name: | Hydroquinone, Octinoxate, and Zinc Oxide |
Active Ingredient(s): | & nbsp; Hydroquinone, Octinoxate, and Zinc Oxide |
Administration Route(s): | |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 62032-513 |
Labeler Name: | OMP, INC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20121107 |
Package NDC: | 62032-513-00 |
Package Description: | 1 KIT in 1 CARTON (62032-513-00) * 198 mL in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC * 198 mL in 1 BOTTLE, PLASTIC * 48 g in 1 BOTTLE, PLASTIC * 85 g in 1 TUBE (62032-104-90) * 57 g in 1 BOTTLE, PLASTIC (62032-101-36) * 57 g in 1 BOTTLE, PLASTIC (62032-100-36) |
NDC Code | 62032-513-00 |
Proprietary Name | NU-DERM SYSTEM NORMAL-OILY |
Package Description | 1 KIT in 1 CARTON (62032-513-00) * 198 mL in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC * 198 mL in 1 BOTTLE, PLASTIC * 48 g in 1 BOTTLE, PLASTIC * 85 g in 1 TUBE (62032-104-90) * 57 g in 1 BOTTLE, PLASTIC (62032-101-36) * 57 g in 1 BOTTLE, PLASTIC (62032-100-36) |
Product NDC | 62032-513 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Hydroquinone, Octinoxate, and Zinc Oxide |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20121107 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | OMP, INC. |
Substance Name | |
Strength Number | |
Strength Unit | |
Pharmaceutical Classes |