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 |