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: | 0023-3459-36 |
Package Description: | 12 POUCH in 1 CARTON (0023-3459-36) > 3 mL in 1 POUCH |
NDC Code | 0023-3459-36 |
Proprietary Name | VIVITE Daily Facial Moisturizer with Sunscreen SPF 30 |
Package Description | 12 POUCH in 1 CARTON (0023-3459-36) > 3 mL in 1 POUCH |
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 |