Prevage Anti Aging Moisture Broad Spectrum Sunscreen SPF 30 is a Topical Lotion in the Human Otc Drug category. It is labeled and distributed by Elizabeth Arden, Inc. The primary component is Octinoxate; Octisalate; Oxybenzone; Octocrylene; Avobenzone.
| Product ID | 67938-0904_9f69f4f0-b49a-4b08-b3fe-691cf0fa03d3 |
| NDC | 67938-0904 |
| Product Type | Human Otc Drug |
| Proprietary Name | Prevage Anti Aging Moisture Broad Spectrum Sunscreen SPF 30 |
| Generic Name | Octinoxate, Octisalate, Oxybenzone, Octocrylene, And Avobenzone |
| Dosage Form | Lotion |
| Route of Administration | TOPICAL |
| Marketing Start Date | 2009-06-04 |
| Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
| Application Number | part352 |
| Labeler Name | Elizabeth Arden, Inc |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE; OCTOCRYLENE; AVOBENZONE |
| Active Ingredient Strength | 35 mg/50mL; mg/50mL; mg/50mL; mg/50mL; mg/50mL |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
| Marketing Start Date | 2009-06-04 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-08-03 |
| Marketing End Date | 2013-04-24 |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2009-06-04 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-08-03 |
| Marketing End Date | 2013-04-24 |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-08-03 |
| Marketing End Date | 2013-04-24 |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-08-03 |
| Marketing End Date | 2013-04-24 |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2009-06-04 |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-08-03 |
| Marketing End Date | 2013-04-24 |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-08-03 |
| Marketing End Date | 2013-04-24 |
| Ingredient | Strength |
|---|---|
| OCTINOXATE | 35 mg/50mL |
| SPL SET ID: | e9cef947-b08b-4fe0-9a65-c8090679608c |
| Manufacturer | |
| UNII |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 67938-0904 | Prevage Anti Aging Moisture Broad Spectrum Sunscreen SPF 30 | OCTINOXATE, OCTISALATE, OXYBENZONE, OCTOCRYLENE, and AVOBENZONE |
| 67938-9144 | Prevage Anti Aging Moisture Broad Spectrum Sunscreen SPF 30 | OCTINOXATE, OCTISALATE, OXYBENZONE, OCTOCRYLENE, and AVOBENZONE |
| 67938-1145 | Ceramide Premier Intense Moisture and Renewal Activation Broad Spectrum SPF 30 | OCTINOXATE, OCTISALATE, OXYBENZONE, OCTOCRYLENE, and AVOBENZONE |