| Product NDC: | 68828-049 |
| Proprietary Name: | JAFRA PRO FACE LIFT |
| Non Proprietary Name: | OCTOCRYLENE OCTISALATE HOMOSALATE AVOBENZONE |
| Active Ingredient(s): | 3; 5; 5; 7 g/100mL; g/100mL; g/100mL; g/100mL & nbsp; OCTOCRYLENE OCTISALATE HOMOSALATE AVOBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 68828-049 |
| Labeler Name: | JAFRA COSMETICS INTERNATIONAL |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120504 |
| Package NDC: | 68828-049-11 |
| Package Description: | 1 BOTTLE in 1 BOX (68828-049-11) > 30 mL in 1 BOTTLE (68828-049-67) |
| NDC Code | 68828-049-11 |
| Proprietary Name | JAFRA PRO FACE LIFT |
| Package Description | 1 BOTTLE in 1 BOX (68828-049-11) > 30 mL in 1 BOTTLE (68828-049-67) |
| Product NDC | 68828-049 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTOCRYLENE OCTISALATE HOMOSALATE AVOBENZONE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120504 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | JAFRA COSMETICS INTERNATIONAL |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE |
| Strength Number | 3; 5; 5; 7 |
| Strength Unit | g/100mL; g/100mL; g/100mL; g/100mL |
| Pharmaceutical Classes |