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Hydrophor
Hydrophor - 54162-500-01 - (Petrolatum)
Drug Information of Hydrophor
| Product NDC: | 54162-500 |
| Proprietary Name: | Hydrophor |
| Non Proprietary Name: | Petrolatum |
| Active Ingredient(s): | 42 g/100g & nbsp; Petrolatum |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydrophor
| Product NDC: | 54162-500 |
| Labeler Name: | Geritrex Corp. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120426 |
Package Information of Hydrophor
| Package NDC: | 54162-500-01 |
| Package Description: | 454 g in 1 JAR (54162-500-01) |
NDC Information of Hydrophor
| NDC Code | 54162-500-01 |
| Proprietary Name | Hydrophor |
| Package Description | 454 g in 1 JAR (54162-500-01) |
| Product NDC | 54162-500 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Petrolatum |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20120426 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Geritrex Corp. |
| Substance Name | PETROLATUM |
| Strength Number | 42 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
