| Product NDC: | 0023-3459 |
| Proprietary Name: | VIVITE Daily Facial Moisturizer with Sunscreen SPF 30 |
| Non Proprietary Name: | octinoxate, octisalate, oxybenzone |
| Active Ingredient(s): | 75; 50; 60 mg/mL; mg/mL; mg/mL & nbsp; octinoxate, octisalate, oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0023-3459 |
| Labeler Name: | Allergan, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20080519 |
| Package NDC: | 0023-3459-50 |
| Package Description: | 1 TUBE in 1 CARTON (0023-3459-50) > 50 mL in 1 TUBE |
| NDC Code | 0023-3459-50 |
| Proprietary Name | VIVITE Daily Facial Moisturizer with Sunscreen SPF 30 |
| Package Description | 1 TUBE in 1 CARTON (0023-3459-50) > 50 mL in 1 TUBE |
| Product NDC | 0023-3459 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | octinoxate, octisalate, oxybenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20080519 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Allergan, Inc. |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 75; 50; 60 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |