| NDC Code | 49967-707-01 |
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| Package Description | 150 mL in 1 BOTTLE, PLASTIC (49967-707-01) |
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| Product NDC | 49967-707 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Kiehls Since 1851 Dermatologist Solutions |
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| Proprietary Name Suffix | Activated Sun Protector Sunscreen Broad Spectrum Spf 50 For Body |
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| Non-Proprietary Name | Avobenzone Homosalate Octisalate Octocrylene Oxybenzone |
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| Dosage Form | LOTION |
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| Usage | TOPICAL |
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| Start Marketing Date | 20120601 |
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| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
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| Application Number | part352 |
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| Manufacturer | L'Oreal USA Products Inc |
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| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
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| Strength | 4.5; 22.5; 7.5; 7.5; 9 |
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| Strength Unit | mL/150mL; mL/150mL; mL/150mL; mL/150mL; mL/150mL |
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