NuGLOWDAYTIME THERAPY With SPF 15 (G.S. COSMECEUTICAL USA, INC.)


Welcome to the PulseAid listing for the NuGLOW drug offered from G.S. COSMECEUTICAL USA, 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: G.S. COSMECEUTICAL USA, INC.
NON-PROPRIETARY NAME: AVOBENZONE, OCTINOXATE, and ZINC OXIDE
SUBSTANCE NAME: AVOBENZONE; OCTINOXATE; ZINC OXIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: CREAM
MARKETING CATEGORY NAME: OTC MONOGRAPH NOT FINAL
START MARKETING DATE: 2010-10-15
END MARKETING DATE: 0000-00-00


NuGLOW DAYTIME THERAPY With SPF 15 HUMAN OTC DRUG Details:

Item DescriptionNuGLOW DAYTIME THERAPY With SPF 15 from G.S. COSMECEUTICAL USA, INC.
LABELER NAME: G.S. COSMECEUTICAL USA, INC.
DEA SCHEDULE:
ACTIVE STRENGTH: 1; 7; 4(g/100g; g/100g; g/100g)
START MARKETING DATE: 2010-10-15
END MARKETING DATE: 0000-00-00
PRODUCT ID: 65113-8503_f895144d-17fd-4efa-8b05-87f986871753
PRODUCT NDC: 65113-8503
APPLICATION NUMBER: part352

Other AVOBENZONE; OCTINOXATE; ZINC OXIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
G.S. COSMECEUTICAL USA, INC.NuGLOW