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Lubriderm Intense Skin Repair
Lubriderm Intense Skin Repair - 58232-0749-1 - (Glycerin)
Drug Information of Lubriderm Intense Skin Repair
| Product NDC: | 58232-0749 |
| Proprietary Name: | Lubriderm Intense Skin Repair |
| Non Proprietary Name: | Glycerin |
| Active Ingredient(s): | 40 mg/g & nbsp; Glycerin |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lubriderm Intense Skin Repair
| Product NDC: | 58232-0749 |
| Labeler Name: | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110131 |
Package Information of Lubriderm Intense Skin Repair
| Package NDC: | 58232-0749-1 |
| Package Description: | 50 g in 1 TUBE (58232-0749-1) |
NDC Information of Lubriderm Intense Skin Repair
| NDC Code | 58232-0749-1 |
| Proprietary Name | Lubriderm Intense Skin Repair |
| Package Description | 50 g in 1 TUBE (58232-0749-1) |
| Product NDC | 58232-0749 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Glycerin |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20110131 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Substance Name | GLYCERIN |
| Strength Number | 40 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
