| NDC Code | 60232-0035-1 |
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| Package Description | 1000 g in 1 TUBE (60232-0035-1) |
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| Product NDC | 60232-0035 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Private Label Spf 50 80 Min Water Resistant |
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| Non-Proprietary Name | Homosalate, Octisalate, Zinc Oxide Sunscreen |
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| Dosage Form | CREAM |
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| Usage | TOPICAL |
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| Start Marketing Date | 20201201 |
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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 | HOMOSALATE; OCTISALATE; ZINC OXIDE |
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| Strength | 100; 50; 165 |
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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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