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Advanced Petrolatum
Advanced Petrolatum - 42213-042-28 - (petrolatum)
Drug Information of Advanced Petrolatum
| Product NDC: | 42213-042 |
| Proprietary Name: | Advanced Petrolatum |
| Non Proprietary Name: | petrolatum |
| Active Ingredient(s): | 1 g/g & nbsp; petrolatum |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Advanced Petrolatum
| Product NDC: | 42213-042 |
| Labeler Name: | Ultra Seal Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110405 |
Package Information of Advanced Petrolatum
| Package NDC: | 42213-042-28 |
| Package Description: | 28 g in 1 TUBE (42213-042-28) |
NDC Information of Advanced Petrolatum
| NDC Code | 42213-042-28 |
| Proprietary Name | Advanced Petrolatum |
| Package Description | 28 g in 1 TUBE (42213-042-28) |
| Product NDC | 42213-042 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | petrolatum |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20110405 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Ultra Seal Corporation |
| Substance Name | PETROLATUM |
| Strength Number | 1 |
| Strength Unit | g/g |
| Pharmaceutical Classes |
