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Aquaphor
Aquaphor - 54868-5870-0 - (Petrolatum)
Drug Information of Aquaphor
| Product NDC: | 54868-5870 |
| Proprietary Name: | Aquaphor |
| Non Proprietary Name: | Petrolatum |
| Active Ingredient(s): | 41 g/100g & nbsp; Petrolatum |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aquaphor
| Product NDC: | 54868-5870 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20080328 |
Package Information of Aquaphor
| Package NDC: | 54868-5870-0 |
| Package Description: | 396 g in 1 JAR (54868-5870-0) |
NDC Information of Aquaphor
| NDC Code | 54868-5870-0 |
| Proprietary Name | Aquaphor |
| Package Description | 396 g in 1 JAR (54868-5870-0) |
| Product NDC | 54868-5870 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Petrolatum |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20080328 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | PETROLATUM |
| Strength Number | 41 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
