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Hydro Skin
Hydro Skin - 0536-5105-97 - (HYDROCORTISONE)
Drug Information of Hydro Skin
| Product NDC: | 0536-5105 |
| Proprietary Name: | Hydro Skin |
| Non Proprietary Name: | HYDROCORTISONE |
| Active Ingredient(s): | 1 g/mL & nbsp; HYDROCORTISONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydro Skin
| Product NDC: | 0536-5105 |
| Labeler Name: | Rugby Laboratories |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20121029 |
Package Information of Hydro Skin
| Package NDC: | 0536-5105-97 |
| Package Description: | 118 mL in 1 BOTTLE (0536-5105-97) |
NDC Information of Hydro Skin
| NDC Code | 0536-5105-97 |
| Proprietary Name | Hydro Skin |
| Package Description | 118 mL in 1 BOTTLE (0536-5105-97) |
| Product NDC | 0536-5105 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HYDROCORTISONE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20121029 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Rugby Laboratories |
| Substance Name | HYDROCORTISONE |
| Strength Number | 1 |
| Strength Unit | g/mL |
| Pharmaceutical Classes |
