| NDC Code | 60232-0008-2 |
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| Package Description | 60 g in 1 BOTTLE (60232-0008-2) |
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| Product NDC | 60232-0008 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Private Label Super Light Oil-free Spf45 |
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| Non-Proprietary Name | 2.75% Octinsalate, 7.50% Octinoxate, 8.00% Zinc Oxide Sunscreen |
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| Dosage Form | LOTION |
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| Usage | TOPICAL |
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| Start Marketing Date | 20110322 |
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| Marketing Category Name | OTC MONOGRAPH DRUG |
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| Application Number | M020 |
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| Manufacturer | Swiss-American CDMO, LLC |
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| Substance Name | OCTINOXATE; OCTISALATE; ZINC OXIDE |
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| Strength | 75; 27.5; 80 |
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| Strength Unit | g/1000g; g/1000g; g/1000g |
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| Pharmacy Classes | Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE] |
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