PRIMEROSE EGF (Royal Springs Cosmetics USA, LLC)


Welcome to the PulseAid listing for the PRIMEROSE EGF drug offered from Royal Springs Cosmetics USA, LLC. 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: Royal Springs Cosmetics USA, LLC
NON-PROPRIETARY NAME: Niacinamide, Dimethicone, Adenosine
SUBSTANCE NAME: NIACINAMIDE; DIMETHICONE; ADENOSINE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: CREAM
MARKETING CATEGORY NAME: UNAPPROVED DRUG OTHER
START MARKETING DATE: 2015-06-08
END MARKETING DATE: 0000-00-00


PRIMEROSE EGF HUMAN OTC DRUG Details:

Item DescriptionPRIMEROSE EGF from Royal Springs Cosmetics USA, LLC
LABELER NAME: Royal Springs Cosmetics USA, LLC
DEA SCHEDULE:
ACTIVE STRENGTH: .02; .015; .0004(1/100mL; 1/100mL; 1/100mL)
START MARKETING DATE: 2015-06-08
END MARKETING DATE: 0000-00-00
PRODUCT ID: 69888-102_5dd04ed9-93ae-4c94-8006-76744e2b4c1b
PRODUCT NDC: 69888-102
APPLICATION NUMBER:

Other NIACINAMIDE; DIMETHICONE; ADENOSINE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Royal Springs Cosmetics USA, LLCPRIMEROSE EGF