MediSpa SunSpraysunblock (Universal Cosmetic Co., Ltd)


Welcome to the PulseAid listing for the MediSpa SunSpray drug offered from Universal Cosmetic 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: Universal Cosmetic Co., Ltd
NON-PROPRIETARY NAME: OCTINOXATE
SUBSTANCE NAME: OCTINOXATE; ENZACAMENE; OCTOCRYLENE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: SPRAY
MARKETING CATEGORY NAME: UNAPPROVED DRUG OTHER
START MARKETING DATE: 2010-08-06
END MARKETING DATE: 0000-00-00


MediSpa SunSpray sunblock HUMAN OTC DRUG Details:

Item DescriptionMediSpa SunSpray sunblock from Universal Cosmetic Co., Ltd
LABELER NAME: Universal Cosmetic Co., Ltd
DEA SCHEDULE:
ACTIVE STRENGTH: .075; .05; .01(mL/mL; mL/mL; mL/mL)
START MARKETING DATE: 2010-08-06
END MARKETING DATE: 0000-00-00
PRODUCT ID: 52554-2001_7dd4f01c-7789-46a4-8617-c0782e79ccdf
PRODUCT NDC: 52554-2001
APPLICATION NUMBER:

Other OCTINOXATE; ENZACAMENE; OCTOCRYLENE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Universal Cosmetic Co., LtdMediSpa SunSpray