| NDC Code | 70764-205-52 |
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| Package Description | 1 TUBE in 1 BOX (70764-205-52) / 74 mL in 1 TUBE (70764-205-22) |
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| Product NDC | 70764-205 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Control Corrective Intensive Skin Brightening |
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| Proprietary Name Suffix | Spf-30 Sunscreen |
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| Non-Proprietary Name | Octinoxate, Octisalate, Zinc Oxide |
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| Dosage Form | CREAM |
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| Usage | TOPICAL |
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| Start Marketing Date | 20180911 |
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| Marketing Category Name | OTC MONOGRAPH FINAL |
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| Application Number | part352 |
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| Manufacturer | CONTROL CORRECTIVE SKINCARE INC |
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| Substance Name | OCTINOXATE; OCTISALATE; ZINC OXIDE |
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| Strength | 6.9; 3; 4 |
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| Strength Unit | g/100mL; g/100mL; g/100mL |
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| Pharmacy Classes | Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE] |
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