| Product NDC: | 50403-999 |
| Proprietary Name: | IQQU Advance Sunscreen |
| Non Proprietary Name: | Dimethicone and Butyl Methoxydibenzoylmethane and Titanium Dioxide and Octyl Methoxycinnamate |
| Active Ingredient(s): | 22; 25; 50; 40 g/mL; g/mL; g/mL; g/mL & nbsp; Dimethicone and Butyl Methoxydibenzoylmethane and Titanium Dioxide and Octyl Methoxycinnamate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 50403-999 |
| Labeler Name: | IQQU USA Co. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100125 |
| Package NDC: | 50403-999-92 |
| Package Description: | 1 TUBE in 1 CARTON (50403-999-92) > 30 mL in 1 TUBE |
| NDC Code | 50403-999-92 |
| Proprietary Name | IQQU Advance Sunscreen |
| Package Description | 1 TUBE in 1 CARTON (50403-999-92) > 30 mL in 1 TUBE |
| Product NDC | 50403-999 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dimethicone and Butyl Methoxydibenzoylmethane and Titanium Dioxide and Octyl Methoxycinnamate |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100125 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | IQQU USA Co. |
| Substance Name | AVOBENZONE; DIMETHICONE; OCTINOXATE; TITANIUM DIOXIDE |
| Strength Number | 22; 25; 50; 40 |
| Strength Unit | g/mL; g/mL; g/mL; g/mL |
| Pharmaceutical Classes |