| Product NDC: | 68572-3004 |
| Proprietary Name: | Karavita Face Essential with SPF 15 |
| Non Proprietary Name: | Octinoxate, Octisalate, and Oxybenzone |
| Active Ingredient(s): | 7.5; 3; 5 g/59mL; g/59mL; g/59mL & nbsp; Octinoxate, Octisalate, and Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 68572-3004 |
| Labeler Name: | Kara Vita, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20040101 |
| Package NDC: | 68572-3004-2 |
| Package Description: | 1 BOTTLE in 1 CARTON (68572-3004-2) > 59 mL in 1 BOTTLE |
| NDC Code | 68572-3004-2 |
| Proprietary Name | Karavita Face Essential with SPF 15 |
| Package Description | 1 BOTTLE in 1 CARTON (68572-3004-2) > 59 mL in 1 BOTTLE |
| Product NDC | 68572-3004 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Octisalate, and Oxybenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20040101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Kara Vita, Inc. |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 7.5; 3; 5 |
| Strength Unit | g/59mL; g/59mL; g/59mL |
| Pharmaceutical Classes |