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NU-DERM Tolereen
NU-DERM Tolereen - 62032-112-36 - (Hydrocortisone)
Drug Information of NU-DERM Tolereen
| Product NDC: | 62032-112 |
| Proprietary Name: | NU-DERM Tolereen |
| Non Proprietary Name: | Hydrocortisone |
| Active Ingredient(s): | 5 mg/g & nbsp; Hydrocortisone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NU-DERM Tolereen
| Product NDC: | 62032-112 |
| Labeler Name: | OMP, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19880101 |
Package Information of NU-DERM Tolereen
| Package NDC: | 62032-112-36 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 BOX (62032-112-36) > 57 g in 1 BOTTLE, PLASTIC |
NDC Information of NU-DERM Tolereen
| NDC Code | 62032-112-36 |
| Proprietary Name | NU-DERM Tolereen |
| Package Description | 1 BOTTLE, PLASTIC in 1 BOX (62032-112-36) > 57 g in 1 BOTTLE, PLASTIC |
| Product NDC | 62032-112 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Hydrocortisone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 19880101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | OMP, Inc. |
| Substance Name | HYDROCORTISONE |
| Strength Number | 5 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
