| Product NDC: | 59158-915 |
| Proprietary Name: | VIRTUAL MATTE |
| Non Proprietary Name: | OCTINOXATE and TITANIUM DIOXIDE |
| Active Ingredient(s): | .02775; .010767 g/mL; g/mL & nbsp; OCTINOXATE and TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 59158-915 |
| Labeler Name: | PRESCRIPTIVES INC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20030901 |
| Package NDC: | 59158-915-01 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (59158-915-01) > 30 mL in 1 BOTTLE, PLASTIC |
| NDC Code | 59158-915-01 |
| Proprietary Name | VIRTUAL MATTE |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (59158-915-01) > 30 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 59158-915 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE and TITANIUM DIOXIDE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20030901 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | PRESCRIPTIVES INC |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
| Strength Number | .02775; .010767 |
| Strength Unit | g/mL; g/mL |
| Pharmaceutical Classes |