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ADVANCED TIME ZONE AGE REVERSING
ADVANCED TIME ZONE AGE REVERSING - 11559-021-01 - (AVOBENZONE, OCTINOXATE, and OCTISALATE)
Drug Information of ADVANCED TIME ZONE AGE REVERSING
| Product NDC: | 11559-021 |
| Proprietary Name: | ADVANCED TIME ZONE AGE REVERSING |
| Non Proprietary Name: | AVOBENZONE, OCTINOXATE, and OCTISALATE |
| Active Ingredient(s): | 3; 7.5; 5 mL/100mL; mL/100mL; mL/100mL & nbsp; AVOBENZONE, OCTINOXATE, and OCTISALATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ADVANCED TIME ZONE AGE REVERSING
| Product NDC: | 11559-021 |
| Labeler Name: | ESTEE LAUDER INC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120601 |
Package Information of ADVANCED TIME ZONE AGE REVERSING
| Package NDC: | 11559-021-01 |
| Package Description: | 1 CONTAINER in 1 CARTON (11559-021-01) > 50 mL in 1 CONTAINER |
NDC Information of ADVANCED TIME ZONE AGE REVERSING
| NDC Code | 11559-021-01 |
| Proprietary Name | ADVANCED TIME ZONE AGE REVERSING |
| Package Description | 1 CONTAINER in 1 CARTON (11559-021-01) > 50 mL in 1 CONTAINER |
| Product NDC | 11559-021 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE, OCTINOXATE, and OCTISALATE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120601 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | ESTEE LAUDER INC |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE |
| Strength Number | 3; 7.5; 5 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
