| NDC Code | 70900-202-54 |
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| Package Description | 1 BOTTLE in 1 BOX (70900-202-54) / 120 mL in 1 BOTTLE (70900-202-14) |
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| Product NDC | 70900-202 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Sunshield |
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| Proprietary Name Suffix | Spf-30 |
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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 | 20160804 |
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| Marketing Category Name | OTC MONOGRAPH FINAL |
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| Application Number | part352 |
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| Manufacturer | CLINICAL CARE SKIN SOLUTIONS, 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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