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NU-DERM SYSTEM NORMAL-DRY
NU-DERM SYSTEM NORMAL-DRY - 62032-516-60 - (Hydroquinone, Octinoxate, and Zinc Oxide)
Drug Information of NU-DERM SYSTEM NORMAL-DRY
| Product NDC: | 62032-516 |
| Proprietary Name: | NU-DERM SYSTEM NORMAL-DRY |
| 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) |
Labeler Information of NU-DERM SYSTEM NORMAL-DRY
| Product NDC: | 62032-516 |
| Labeler Name: | OMP, INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20121107 |
Package Information of NU-DERM SYSTEM NORMAL-DRY
| Package NDC: | 62032-516-60 |
| Package Description: | 1 KIT in 1 CARTON (62032-516-60) * 28 g in 1 TUBE (62032-104-10) * 59 mL in 1 BOTTLE, PLASTIC * 59 mL in 1 BOTTLE, PLASTIC * 28 g in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC (62032-101-36) * 28.5 g in 1 BOTTLE, PLASTIC (62032-100-10) |
NDC Information of NU-DERM SYSTEM NORMAL-DRY
| NDC Code | 62032-516-60 |
| Proprietary Name | NU-DERM SYSTEM NORMAL-DRY |
| Package Description | 1 KIT in 1 CARTON (62032-516-60) * 28 g in 1 TUBE (62032-104-10) * 59 mL in 1 BOTTLE, PLASTIC * 59 mL in 1 BOTTLE, PLASTIC * 28 g in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC (62032-101-36) * 28.5 g in 1 BOTTLE, PLASTIC (62032-100-10) |
| Product NDC | 62032-516 |
| 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 |
