Product NDC: | 11559-035 |
Proprietary Name: | ADVANCED TIME ZONE AGE REVERSING |
Non Proprietary Name: | AVOBENZONE, OCTINOXATE, and OCTISALATE |
Active Ingredient(s): | .03; .075; .05 g/mL; g/mL; g/mL & nbsp; AVOBENZONE, OCTINOXATE, and OCTISALATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11559-035 |
Labeler Name: | ESTEE LAUDER INC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130501 |
Package NDC: | 11559-035-01 |
Package Description: | 1 CONTAINER in 1 CARTON (11559-035-01) > 50 mL in 1 CONTAINER |
NDC Code | 11559-035-01 |
Proprietary Name | ADVANCED TIME ZONE AGE REVERSING |
Package Description | 1 CONTAINER in 1 CARTON (11559-035-01) > 50 mL in 1 CONTAINER |
Product NDC | 11559-035 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | AVOBENZONE, OCTINOXATE, and OCTISALATE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20130501 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | ESTEE LAUDER INC |
Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE |
Strength Number | .03; .075; .05 |
Strength Unit | g/mL; g/mL; g/mL |
Pharmaceutical Classes |