BEEVENOM SUNSPF50PLUS PA PLUS PLUS PLUS (NATURE REPUBLIC CO., LTD.)
Welcome to the PulseAid listing for the BEEVENOM 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, TITANIUM DIOXIDE, OCTISALATE |
SUBSTANCE NAME: | OCTINOXATE; TITANIUM DIOXIDE; OCTISALATE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | CREAM |
MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
START MARKETING DATE: | 2012-02-01 |
END MARKETING DATE: | 0000-00-00 |
BEEVENOM SUN SPF50PLUS PA PLUS PLUS PLUS HUMAN OTC DRUG Details:
Item Description | BEEVENOM SUN SPF50PLUS PA PLUS PLUS PLUS from NATURE REPUBLIC CO., LTD. |
LABELER NAME: | NATURE REPUBLIC CO., LTD. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 3.75; 2.15; 1(g/50mL; g/50mL; g/50mL) |
START MARKETING DATE: | 2012-02-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 51346-023_0efafa1c-d52b-4d45-920c-cbae86f5b1ee |
PRODUCT NDC: | 51346-023 |
APPLICATION NUMBER: | part352 |
Other OCTINOXATE; TITANIUM DIOXIDE; OCTISALATE Pharmaceutical Manufacturers / Labelers: