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) |
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 NDC: | 42213-042-80 |
Package Description: | 144 PACKET in 1 BOX (42213-042-80) > 5 g in 1 PACKET (42213-042-05) |
NDC Code | 42213-042-80 |
Proprietary Name | Advanced Petrolatum |
Package Description | 144 PACKET in 1 BOX (42213-042-80) > 5 g in 1 PACKET (42213-042-05) |
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 |