Forever Sun Lips (Aloe Vera of America, Inc.)


Welcome to the PulseAid listing for the Forever Sun Lips drug offered from Aloe Vera of America, Inc.. This pharmaceutical is classified as a HUMAN OTC DRUG. Below, you can view the 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: Sunscreen
SUBSTANCE NAME: AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; PETROLATUM
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: LIPSTICK
MARKETING CATEGORY NAME: OTC MONOGRAPH NOT FINAL
START MARKETING DATE: 2014-04-25
END MARKETING DATE: 0000-00-00


Forever Sun Lips HUMAN OTC DRUG Details:

Item DescriptionForever Sun Lips from Aloe Vera of America, Inc.
LABELER NAME: Aloe Vera of America, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: .1275; .425; .2125; .1186; 1.615(g/4.25g; g/4.25g; g/4.25g; g/4.25g; g/4.25g)
START MARKETING DATE: 2014-04-25
END MARKETING DATE: 0000-00-00
PRODUCT ID: 11697-462_6c629c19-639c-4c7f-a69f-e7fbbce5cee9
PRODUCT NDC: 11697-462
APPLICATION NUMBER: part352

Other AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; PETROLATUM Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Aloe Vera of America, Inc.Forever Sun Lips