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GenRx Ultra Therapeutic Skin Repairing
GenRx Ultra Therapeutic Skin Repairing - 59088-663-08 - (Dimethicone)
Drug Information of GenRx Ultra Therapeutic Skin Repairing
| Product NDC: | 59088-663 |
| Proprietary Name: | GenRx Ultra Therapeutic Skin Repairing |
| Non Proprietary Name: | Dimethicone |
| Active Ingredient(s): | 50 mg/mL & nbsp; Dimethicone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of GenRx Ultra Therapeutic Skin Repairing
| Product NDC: | 59088-663 |
| Labeler Name: | PureTek Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130108 |
Package Information of GenRx Ultra Therapeutic Skin Repairing
| Package NDC: | 59088-663-08 |
| Package Description: | 118 mL in 1 TUBE (59088-663-08) |
NDC Information of GenRx Ultra Therapeutic Skin Repairing
| NDC Code | 59088-663-08 |
| Proprietary Name | GenRx Ultra Therapeutic Skin Repairing |
| Package Description | 118 mL in 1 TUBE (59088-663-08) |
| Product NDC | 59088-663 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dimethicone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130108 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | PureTek Corporation |
| Substance Name | DIMETHICONE |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
