SHISEIDO SUN PROTECTION EYE (SHISEIDO AMERICA INC.)
Welcome to the PulseAid listing for the SHISEIDO SUN PROTECTION EYE drug offered from SHISEIDO AMERICA 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: | SHISEIDO AMERICA INC. |
NON-PROPRIETARY NAME: | OCTINOXATE, OCTOCRYLENE, and ZINC OXIDE |
SUBSTANCE NAME: | OCTINOXATE; OCTOCRYLENE; ZINC OXIDE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | CREAM |
MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
START MARKETING DATE: | 2012-12-01 |
END MARKETING DATE: | 0000-00-00 |
SHISEIDO SUN PROTECTION EYE HUMAN OTC DRUG Details:
Item Description | SHISEIDO SUN PROTECTION EYE from SHISEIDO AMERICA INC. |
LABELER NAME: | SHISEIDO AMERICA INC. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 479; 495; 1749(mg/16.5g; mg/16.5g; mg/16.5g) |
START MARKETING DATE: | 2012-12-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 52686-335_0801ab22-8145-4711-b95c-3b786b1ceafb |
PRODUCT NDC: | 52686-335 |
APPLICATION NUMBER: | part352 |
Other OCTINOXATE; OCTOCRYLENE; ZINC OXIDE Pharmaceutical Manufacturers / Labelers: