Product NDC: | 0168-0053 |
Proprietary Name: | White Petrolatum |
Non Proprietary Name: | White Petrolatum |
Active Ingredient(s): | 1 g/g & nbsp; White Petrolatum |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0168-0053 |
Labeler Name: | E. Fougera & Co. a division of Fougera Pharmaceuticals Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part347 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19680101 |
Package NDC: | 0168-0053-45 |
Package Description: | 1 PACKET in 1 CARTON (0168-0053-45) > 5 g in 1 PACKET |
NDC Code | 0168-0053-45 |
Proprietary Name | White Petrolatum |
Package Description | 1 PACKET in 1 CARTON (0168-0053-45) > 5 g in 1 PACKET |
Product NDC | 0168-0053 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | White Petrolatum |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 19680101 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | E. Fougera & Co. a division of Fougera Pharmaceuticals Inc. |
Substance Name | PETROLATUM |
Strength Number | 1 |
Strength Unit | g/g |
Pharmaceutical Classes |