Sun Protection Emulsion Face Broad Spectrum SPF 30La Prairie Group (La Prairie Group AG)
Welcome to the PulseAid listing for the Sun Protection Emulsion Face Broad Spectrum SPF 30 drug offered from La Prairie Group AG. This pharmaceutical is classified as a HUMAN OTC DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN OTC DRUG drug type category.
| LABELER NAME / MANUFACTURER: | La Prairie Group AG |
| NON-PROPRIETARY NAME: | Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone |
| SUBSTANCE NAME: | HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE; AVOBENZONE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | CREAM |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
| START MARKETING DATE: | 2011-02-14 |
| END MARKETING DATE: | 0000-00-00 |
Sun Protection Emulsion Face Broad Spectrum SPF 30 La Prairie Group HUMAN OTC DRUG Details:
| Item Description | Sun Protection Emulsion Face Broad Spectrum SPF 30 La Prairie Group from La Prairie Group AG |
| LABELER NAME: | La Prairie Group AG |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 10; 2.6; 2.4; 5; 3(g/100mL; g/100mL; g/100mL; g/100mL; g/100mL) |
| START MARKETING DATE: | 2011-02-14 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 76157-222_0113a2f9-6be2-4c41-a85b-7fe1b20647ad |
| PRODUCT NDC: | 76157-222 |
| APPLICATION NUMBER: | part352 |
Other HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE; AVOBENZONE Pharmaceutical Manufacturers / Labelers:
