Product NDC: | 42472-002 |
Proprietary Name: | LAB SERIES SKINCARE FOR MEN |
Non Proprietary Name: | OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE, and ZINC OXIDE |
Active Ingredient(s): | 7.4; 4; 2.5; 2.2; 2 mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE, and ZINC OXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42472-002 |
Labeler Name: | Aramis Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110424 |
Package NDC: | 42472-002-01 |
Package Description: | 1 BOTTLE in 1 CARTON (42472-002-01) > 50 mL in 1 BOTTLE |
NDC Code | 42472-002-01 |
Proprietary Name | LAB SERIES SKINCARE FOR MEN |
Package Description | 1 BOTTLE in 1 CARTON (42472-002-01) > 50 mL in 1 BOTTLE |
Product NDC | 42472-002 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE, and ZINC OXIDE |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20110424 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Aramis Inc. |
Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE; TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | 7.4; 4; 2.5; 2.2; 2 |
Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL |
Pharmaceutical Classes |