Lagom Cellus Sun Gel (SKINMED International Co., Ltd.)


Welcome to the PulseAid listing for the Lagom Cellus Sun Gel drug offered from SKINMED International 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: SKINMED International Co., Ltd.
NON-PROPRIETARY NAME: OCTINOXATE, OCTOCRYLENE, OCTISALATE
SUBSTANCE NAME: OCTINOXATE; OCTOCRYLENE; OCTISALATE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: GEL
MARKETING CATEGORY NAME: OTC MONOGRAPH NOT FINAL
START MARKETING DATE: 2016-06-13
END MARKETING DATE: 0000-00-00


Lagom Cellus Sun Gel HUMAN OTC DRUG Details:

Item DescriptionLagom Cellus Sun Gel from SKINMED International Co., Ltd.
LABELER NAME: SKINMED International Co., Ltd.
DEA SCHEDULE:
ACTIVE STRENGTH: 3.5; 2.5; 2(mg/50mL; mg/50mL; mg/50mL)
START MARKETING DATE: 2016-06-13
END MARKETING DATE: 0000-00-00
PRODUCT ID: 70738-001_4b40f645-736c-4f5e-a58b-77ad657cc4aa
PRODUCT NDC: 70738-001
APPLICATION NUMBER: part352

Other OCTINOXATE; OCTOCRYLENE; OCTISALATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Codecosme International Co., Ltd.Multi Protection UV Bouncer
SKINMED International Co., Ltd.Lagom Cellus Sun Gel
The Saem International Co., Ltd.ECO EARTH POWER Aqua Sun