| 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: | 0168-0053-21 |
| Package Description: | 1 TUBE in 1 CARTON (0168-0053-21) > 28.35 g in 1 TUBE |
| NDC Code | 0168-0053-21 |
| Proprietary Name | White Petrolatum |
| Package Description | 1 TUBE in 1 CARTON (0168-0053-21) > 28.35 g in 1 TUBE |
| 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 |