THE FIRST SUNSPF50 PLUS PA PLUS PLUS PLUS (NATURE REPUBLIC CO., LTD.)
Welcome to the PulseAid listing for the THE FIRST SUN drug offered from NATURE REPUBLIC CO., LTD.. 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: | NATURE REPUBLIC CO., LTD. |
NON-PROPRIETARY NAME: | OCTINOXATE, ZINC OXIDE, OCTISALATE, TITANIUM DIOXIDE |
SUBSTANCE NAME: | OCTINOXATE; ZINC OXIDE; OCTISALATE; TITANIUM DIOXIDE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | LIQUID |
MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
START MARKETING DATE: | 2012-03-01 |
END MARKETING DATE: | 0000-00-00 |
THE FIRST SUN SPF50 PLUS PA PLUS PLUS PLUS HUMAN OTC DRUG Details:
Item Description | THE FIRST SUN SPF50 PLUS PA PLUS PLUS PLUS from NATURE REPUBLIC CO., LTD. |
LABELER NAME: | NATURE REPUBLIC CO., LTD. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 3; 2.61; 2; 1(g/40mL; g/40mL; g/40mL; g/40mL) |
START MARKETING DATE: | 2012-03-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 51346-001_eba63df1-32eb-4b62-95a2-995fb5973663 |
PRODUCT NDC: | 51346-001 |
APPLICATION NUMBER: | part352 |
Other OCTINOXATE; ZINC OXIDE; OCTISALATE; TITANIUM DIOXIDE Pharmaceutical Manufacturers / Labelers: