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 |