Avon SunSunscreen Face (Avon Products, Inc)
Welcome to the PulseAid listing for the Avon Sun drug offered from Avon Products, Inc. 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: | Avon Products, Inc |
NON-PROPRIETARY NAME: | Homosalate, Oxybenzone, Octisalate, Avobenzone, Octocrylene |
SUBSTANCE NAME: | HOMOSALATE; OXYBENZONE; OCTISALATE; AVOBENZONE; OCTOCRYLENE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | LOTION |
MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
START MARKETING DATE: | 2013-03-26 |
END MARKETING DATE: | 0000-00-00 |
Avon Sun Sunscreen Face HUMAN OTC DRUG Details:
Item Description | Avon Sun Sunscreen Face from Avon Products, Inc |
LABELER NAME: | Avon Products, Inc |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 95; 60; 47.5; 30; 28(mg/mL; mg/mL; mg/mL; mg/mL; mg/mL) |
START MARKETING DATE: | 2013-03-26 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 10096-0294_017eb0fc-896b-44a7-998f-d494e7a844e8 |
PRODUCT NDC: | 10096-0294 |
APPLICATION NUMBER: | part352 |
Other HOMOSALATE; OXYBENZONE; OCTISALATE; AVOBENZONE; OCTOCRYLENE Pharmaceutical Manufacturers / Labelers: