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 DescriptionAloe Sunscreen from Aloe Vera of America, Inc.
LABELER NAME: Aloe Vera of America, Inc.
DEA SCHEDULE:
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:

Manufacturer / LabelerProprietary Name
Aloe Vera of America, Inc.Aloe Sunscreen