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 Description | NuGLOW DAYTIME THERAPY With SPF 15 from G.S. COSMECEUTICAL USA, INC. |
LABELER NAME: | G.S. COSMECEUTICAL USA, INC. |
DEA SCHEDULE: |
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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: