| Product NDC: | 67938-1044 |
| Proprietary Name: | Intervene Radiance Boosting Moisture SPF 15 |
| Non Proprietary Name: | Octinoxate |
| Active Ingredient(s): | 1.5; 3.75; 1.5 g/50g; g/50g; g/50g & nbsp; Octinoxate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 67938-1044 |
| Labeler Name: | Elizabeth Arden, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090727 |
| Package NDC: | 67938-1044-3 |
| Package Description: | 1 TUBE in 1 BOX (67938-1044-3) > 15 g in 1 TUBE (67938-1044-4) |
| NDC Code | 67938-1044-3 |
| Proprietary Name | Intervene Radiance Boosting Moisture SPF 15 |
| Package Description | 1 TUBE in 1 BOX (67938-1044-3) > 15 g in 1 TUBE (67938-1044-4) |
| Product NDC | 67938-1044 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20090727 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Elizabeth Arden, Inc |
| Substance Name | AVOBENZONE; OCTINOXATE; OXYBENZONE |
| Strength Number | 1.5; 3.75; 1.5 |
| Strength Unit | g/50g; g/50g; g/50g |
| Pharmaceutical Classes |