| NDC Code | 70738-001-02 |
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| Package Description | 1 CONTAINER in 1 PACKAGE (70738-001-02) > 50 mL in 1 CONTAINER (70738-001-01) |
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| Product NDC | 70738-001 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Lagom Cellus Sun Gel |
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| Non-Proprietary Name | Octinoxate, Octocrylene, Octisalate |
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| Dosage Form | GEL |
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| Usage | TOPICAL |
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| Start Marketing Date | 20180108 |
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| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
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| Application Number | part352 |
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| Manufacturer | SKINMED International Co., Ltd. |
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| Substance Name | OCTINOXATE; OCTOCRYLENE; OCTISALATE |
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| Strength | 3.5; 2.5; 2 |
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| Strength Unit | mg/50mL; mg/50mL; mg/50mL |
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