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 |