| NDC Code | 76344-2001-2 |
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| Package Description | 1 BOTTLE, WITH APPLICATOR in 1 BOX (76344-2001-2) > 55 mL in 1 BOTTLE, WITH APPLICATOR (76344-2001-1) |
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| Product NDC | 76344-2001 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Medispa Sunspray (sunblock) |
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| Non-Proprietary Name | Octinoxate, Amiloxate, Bemotrizinol, Titanium Dioxide |
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| Dosage Form | SPRAY |
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| Usage | TOPICAL |
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| Start Marketing Date | 20130329 |
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| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
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| Application Number | part352 |
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| Manufacturer | Humex,Inc. |
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| Substance Name | AMILOXATE; BEMOTRIZINOL; OCTINOXATE; TITANIUM DIOXIDE |
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| Strength | 2; 2; 7.5; 1.4 |
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| Strength Unit | g/100mL; g/100mL; g/100mL; g/100mL |
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