| Product NDC: | 68570-744 |
| Proprietary Name: | shu uemura UV under base mousse |
| Non Proprietary Name: | Octinoxate Octisalate Octocrylene Titanium Dioxide |
| Active Ingredient(s): | 4.6; 3.1; 1.9; 3.1 g/65g; g/65g; g/65g; g/65g & nbsp; Octinoxate Octisalate Octocrylene Titanium Dioxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | AEROSOL, FOAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 68570-744 |
| Labeler Name: | Cosmelor Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100201 |
| Package NDC: | 68570-744-01 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (68570-744-01) > 65 g in 1 BOTTLE, PUMP |
| NDC Code | 68570-744-01 |
| Proprietary Name | shu uemura UV under base mousse |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (68570-744-01) > 65 g in 1 BOTTLE, PUMP |
| Product NDC | 68570-744 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate Octisalate Octocrylene Titanium Dioxide |
| Dosage Form Name | AEROSOL, FOAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Cosmelor Ltd |
| Substance Name | OCTINOXATE; OCTISALATE; OCTOCRYLENE; TITANIUM DIOXIDE |
| Strength Number | 4.6; 3.1; 1.9; 3.1 |
| Strength Unit | g/65g; g/65g; g/65g; g/65g |
| Pharmaceutical Classes |