| NDC Code | 84066-109-01 |
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| Package Description | 50 g in 1 BOTTLE (84066-109-01) |
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| Product NDC | 84066-109 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Medultima Adventure Sunscreen |
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| Non-Proprietary Name | Homosalate,octocrylene, Phenylbenzimidazole Sulfonic Acid, Ethylhexyl Salicylate, Butyl Methoxydibenzoylmethane |
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| Dosage Form | CREAM |
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| Usage | TOPICAL |
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| Start Marketing Date | 20260604 |
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| Marketing Category Name | OTC MONOGRAPH DRUG |
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| Application Number | M020 |
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| Manufacturer | Guangzhou Tata Biotechnology Co., Ltd. |
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| Substance Name | BUTYL METHOXYDIBENZOYLMETHANE; ETHYLHEXYL SALICYLATE; HOMOSALATE; OCTOCRYLENE; PHENYLBENZIMIDAZOLE SULFONIC ACID |
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| Strength | 3; 4; 9; 7; 4 |
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| Strength Unit | g/100g; g/100g; g/100g; g/100g; g/100g |
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