| Product NDC: | 49527-743 |
| Proprietary Name: | LONG LAST GLOSSWEAR |
| Non Proprietary Name: | OCTINOXATE, OCTISALATE |
| Active Ingredient(s): | 7.5; 4 mL/100mL; mL/100mL & nbsp; OCTINOXATE, OCTISALATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49527-743 |
| Labeler Name: | CLINIQUE LABORATORIES INC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20080301 |
| Package NDC: | 49527-743-01 |
| Package Description: | 1 TUBE, WITH APPLICATOR in 1 CARTON (49527-743-01) > 6 mL in 1 TUBE, WITH APPLICATOR (49527-743-02) |
| NDC Code | 49527-743-01 |
| Proprietary Name | LONG LAST GLOSSWEAR |
| Package Description | 1 TUBE, WITH APPLICATOR in 1 CARTON (49527-743-01) > 6 mL in 1 TUBE, WITH APPLICATOR (49527-743-02) |
| Product NDC | 49527-743 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OCTISALATE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20080301 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | CLINIQUE LABORATORIES INC |
| Substance Name | OCTINOXATE; OCTISALATE |
| Strength Number | 7.5; 4 |
| Strength Unit | mL/100mL; mL/100mL |
| Pharmaceutical Classes |