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Dermarest
Dermarest - 63736-339-24 - (Hydrocortisone)
Drug Information of Dermarest
| Product NDC: | 63736-339 |
| Proprietary Name: | Dermarest |
| Non Proprietary Name: | Hydrocortisone |
| Active Ingredient(s): | 1.18 mL/118mL & nbsp; Hydrocortisone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dermarest
| Product NDC: | 63736-339 |
| Labeler Name: | Insight Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100920 |
Package Information of Dermarest
| Package NDC: | 63736-339-24 |
| Package Description: | 24 CARTON in 1 CASE (63736-339-24) > 1 BOTTLE in 1 CARTON > 118 mL in 1 BOTTLE |
NDC Information of Dermarest
| NDC Code | 63736-339-24 |
| Proprietary Name | Dermarest |
| Package Description | 24 CARTON in 1 CASE (63736-339-24) > 1 BOTTLE in 1 CARTON > 118 mL in 1 BOTTLE |
| Product NDC | 63736-339 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Hydrocortisone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100920 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Insight Pharmaceuticals |
| Substance Name | HYDROCORTISONE |
| Strength Number | 1.18 |
| Strength Unit | mL/118mL |
| Pharmaceutical Classes |
