| Product NDC: | 64942-1190 |
| Proprietary Name: | Vaseline |
| Non Proprietary Name: | OCTISALATE, AVOBENZONE, ENSULIZOLE |
| Active Ingredient(s): | 20; 15; 50; 13 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; OCTISALATE, AVOBENZONE, ENSULIZOLE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 64942-1190 |
| Labeler Name: | CONOPCO Inc. d/b/a Unilever |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120801 |
| Package NDC: | 64942-1190-1 |
| Package Description: | 600 mL in 1 BOTTLE (64942-1190-1) |
| NDC Code | 64942-1190-1 |
| Proprietary Name | Vaseline |
| Package Description | 600 mL in 1 BOTTLE (64942-1190-1) |
| Product NDC | 64942-1190 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTISALATE, AVOBENZONE, ENSULIZOLE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120801 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | CONOPCO Inc. d/b/a Unilever |
| Substance Name | AVOBENZONE; ENSULIZOLE; OCTISALATE; OCTOCRYLENE |
| Strength Number | 20; 15; 50; 13 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |