| Product NDC: | 0023-4383 |
| Proprietary Name: | VIVITE Aftercare Environmental Protection Sunscreen SPF 30 |
| Non Proprietary Name: | octinoxate, octisalate, zinc oxide |
| Active Ingredient(s): | 75; 40; 78 mg/g; mg/g; mg/g & nbsp; octinoxate, octisalate, zinc oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0023-4383 |
| Labeler Name: | Allergan, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111015 |
| Package NDC: | 0023-4383-32 |
| Package Description: | 907 g in 1 BOTTLE, PUMP (0023-4383-32) |
| NDC Code | 0023-4383-32 |
| Proprietary Name | VIVITE Aftercare Environmental Protection Sunscreen SPF 30 |
| Package Description | 907 g in 1 BOTTLE, PUMP (0023-4383-32) |
| Product NDC | 0023-4383 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | octinoxate, octisalate, zinc oxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20111015 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Allergan, Inc. |
| Substance Name | OCTINOXATE; OCTISALATE; ZINC OXIDE |
| Strength Number | 75; 40; 78 |
| Strength Unit | mg/g; mg/g; mg/g |
| Pharmaceutical Classes |