Tahitian NoniSunscreen (Wasatch Product Development)
Welcome to the PulseAid listing for the Tahitian Noni drug offered from Wasatch Product Development. 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: | Wasatch Product Development |
NON-PROPRIETARY NAME: | Avobenzone, Homosalate, Octinoxate, Octisalate, Oxybenzone |
SUBSTANCE NAME: | AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | LOTION |
MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
START MARKETING DATE: | 2010-06-28 |
END MARKETING DATE: | 0000-00-00 |
Tahitian Noni Sunscreen HUMAN OTC DRUG Details:
Item Description | Tahitian Noni Sunscreen from Wasatch Product Development |
LABELER NAME: | Wasatch Product Development |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 2; 6.5; 7; 5; 3(mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL) |
START MARKETING DATE: | 2010-06-28 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 44717-536_1ef931a4-35c1-4f41-a2c1-08c5b835a8fe |
PRODUCT NDC: | 44717-536 |
APPLICATION NUMBER: | part352 |
Other AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE Pharmaceutical Manufacturers / Labelers: