Product NDC: | 68327-003 |
Proprietary Name: | Skin Tint FX |
Non Proprietary Name: | OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE, ZINC OXIDE |
Active Ingredient(s): | 6.5; 3.5; 2.1; 5.5; 5.5 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL & nbsp; OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE, ZINC OXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68327-003 |
Labeler Name: | Cover FX Skin Care, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110920 |
Package NDC: | 68327-003-01 |
Package Description: | 30 mL in 1 TUBE (68327-003-01) |
NDC Code | 68327-003-01 |
Proprietary Name | Skin Tint FX |
Package Description | 30 mL in 1 TUBE (68327-003-01) |
Product NDC | 68327-003 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE, ZINC OXIDE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20110920 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Cover FX Skin Care, Inc. |
Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE; TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | 6.5; 3.5; 2.1; 5.5; 5.5 |
Strength Unit | g/100mL; g/100mL; g/100mL; g/100mL; g/100mL |
Pharmaceutical Classes |