Product NDC: | 64942-1048 |
Proprietary Name: | Vaseline Intensive Care |
Non Proprietary Name: | SPF 15 |
Active Ingredient(s): | 7.5; 1; 3 mL/100mL; mL/100mL; mL/100mL & nbsp; SPF 15 |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64942-1048 |
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: | 20081223 |
Package NDC: | 64942-1048-1 |
Package Description: | 600 mL in 1 BOTTLE (64942-1048-1) |
NDC Code | 64942-1048-1 |
Proprietary Name | Vaseline Intensive Care |
Package Description | 600 mL in 1 BOTTLE (64942-1048-1) |
Product NDC | 64942-1048 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | SPF 15 |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20081223 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Conopco Inc. d/b/a Unilever |
Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE |
Strength Number | 7.5; 1; 3 |
Strength Unit | mL/100mL; mL/100mL; mL/100mL |
Pharmaceutical Classes |