NU-DERM SUNFADERSkin Lightener with Sunscreen (SPF 15) PABA FREE (OMP, INC.)


Welcome to the PulseAid listing for the NU-DERM SUNFADER drug offered from OMP, INC.. This Depigmenting Activity [PE],Melanin Synthesis Inhibitor [EPC],Melanin Synthesis Inhibitors [MoA] pharmaceutical is classified as a HUMAN PRESCRIPTION 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 PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: OMP, INC.
NON-PROPRIETARY NAME: HYDROQUINONE, OCTINOXATE, and OXYBENZONE
SUBSTANCE NAME: HYDROQUINONE; OCTINOXATE; OXYBENZONE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Depigmenting Activity [PE],Melanin Synthesis Inhibitor [EPC],Melanin Synthesis Inhibitors [MoA]
ROUTE: TOPICAL
DOSAGE FORM: LOTION
MARKETING CATEGORY NAME: UNAPPROVED DRUG OTHER
START MARKETING DATE: 1984-01-01
END MARKETING DATE: 0000-00-00


NU-DERM SUNFADER Skin Lightener with Sunscreen (SPF 15) PABA FREE HUMAN PRESCRIPTION DRUG Details:

Item DescriptionNU-DERM SUNFADER Skin Lightener with Sunscreen (SPF 15) PABA FREE from OMP, INC.
LABELER NAME: OMP, INC.
DEA SCHEDULE:
ACTIVE STRENGTH: 40; 75; 55(mg/g; mg/g; mg/g)
START MARKETING DATE: 1984-01-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 62032-116_5340a775-399e-4233-a30d-e4e872023d3f
PRODUCT NDC: 62032-116
APPLICATION NUMBER:

Other HYDROQUINONE; OCTINOXATE; OXYBENZONE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
OMP, INC.NU-DERM SUNFADER