Aloe Sunscreen (Aloe Vera of America, Inc.)
Welcome to the PulseAid listing for the Aloe Sunscreen drug offered from Aloe Vera of America, 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: | Aloe Vera of America, Inc. |
NON-PROPRIETARY NAME: | Homosalate, Octisalate, Avobenzone, Ensulizole and Octocrylene |
SUBSTANCE NAME: | HOMOSALATE; OCTISALATE; AVOBENZONE; ENSULIZOLE; OCTOCRYLENE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | LOTION |
MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
START MARKETING DATE: | 2011-04-06 |
END MARKETING DATE: | 0000-00-00 |
Aloe Sunscreen HUMAN OTC DRUG Details:
Item Description | Aloe Sunscreen from Aloe Vera of America, Inc. |
LABELER NAME: | Aloe Vera of America, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 10; 5; 2.5; 3; 2.79(g/100mL; g/100mL; g/100mL; g/100mL; g/100mL) |
START MARKETING DATE: | 2011-04-06 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 11697-199_6f7c5e65-6ad1-431f-a801-7aa79fd40926 |
PRODUCT NDC: | 11697-199 |
APPLICATION NUMBER: | part352 |
Other HOMOSALATE; OCTISALATE; AVOBENZONE; ENSULIZOLE; OCTOCRYLENE Pharmaceutical Manufacturers / Labelers: