| Product NDC: | 64942-1290 |
| Proprietary Name: | Simple |
| Non Proprietary Name: | AVOBENZONE, ENSULIZOLE, OCTICSALATE |
| Active Ingredient(s): | 3; 1; 5 g/100mL; g/100mL; g/100mL & nbsp; AVOBENZONE, ENSULIZOLE, OCTICSALATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 64942-1290 |
| 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: | 20130701 |
| Package NDC: | 64942-1290-2 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (64942-1290-2) > 124 mL in 1 BOTTLE, PLASTIC (64942-1290-1) |
| NDC Code | 64942-1290-2 |
| Proprietary Name | Simple |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (64942-1290-2) > 124 mL in 1 BOTTLE, PLASTIC (64942-1290-1) |
| Product NDC | 64942-1290 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE, ENSULIZOLE, OCTICSALATE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20130701 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | CONOPCO Inc. d/b/a Unilever |
| Substance Name | AVOBENZONE; ENSULIZOLE; OCTISALATE |
| Strength Number | 3; 1; 5 |
| Strength Unit | g/100mL; g/100mL; g/100mL |
| Pharmaceutical Classes |