| 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 |