| 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 |