Neova DNA Damage Control – EverydaySPF 43 (PhotoMedex, Inc.)
Welcome to the PulseAid listing for the Neova DNA Damage Control – Everyday drug offered from PhotoMedex, 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: | PhotoMedex, Inc. |
NON-PROPRIETARY NAME: | Zinc Oxide, Octinoxate, Octisalate |
SUBSTANCE NAME: | ZINC OXIDE; OCTINOXATE; OCTISALATE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | EMULSION |
MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
START MARKETING DATE: | 2012-01-06 |
END MARKETING DATE: | 0000-00-00 |
Neova DNA Damage Control – Everyday SPF 43 HUMAN OTC DRUG Details:
Item Description | Neova DNA Damage Control – Everyday SPF 43 from PhotoMedex, Inc. |
LABELER NAME: | PhotoMedex, Inc. |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 7.5; 7.5; 2.5(mL/100mL; mL/100mL; mL/100mL) |
START MARKETING DATE: | 2012-01-06 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 62362-139_9434e317-85ce-44f4-ac99-dbe37d5f6b6c |
PRODUCT NDC: | 62362-139 |
APPLICATION NUMBER: | part352 |
Other ZINC OXIDE; OCTINOXATE; OCTISALATE Pharmaceutical Manufacturers / Labelers: