| Product NDC: | 11559-026 |
| Proprietary Name: | DAY WEAR ADVANCED MULTI-PROTECTION ANTI-OXIDANT AND UV DEFENSE |
| Non Proprietary Name: | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, and OXYBENZONE |
| Active Ingredient(s): | .0312; .052; .052; .02808; .0312 g/mL; g/mL; g/mL; g/mL; g/mL & nbsp; AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, and OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 11559-026 |
| Labeler Name: | ESTEE LAUDER INC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20121107 |
| Package NDC: | 11559-026-01 |
| Package Description: | 1 BOTTLE in 1 CARTON (11559-026-01) > 30 mL in 1 BOTTLE |
| NDC Code | 11559-026-01 |
| Proprietary Name | DAY WEAR ADVANCED MULTI-PROTECTION ANTI-OXIDANT AND UV DEFENSE |
| Package Description | 1 BOTTLE in 1 CARTON (11559-026-01) > 30 mL in 1 BOTTLE |
| Product NDC | 11559-026 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, and OXYBENZONE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20121107 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | ESTEE LAUDER INC |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | .0312; .052; .052; .02808; .0312 |
| Strength Unit | g/mL; g/mL; g/mL; g/mL; g/mL |
| Pharmaceutical Classes |