GLAMTOX ACTIVE DAILY MOISTURIZING SUNSCREEN (Rodial, Ltd.)


Welcome to the PulseAid listing for the GLAMTOX ACTIVE DAILY MOISTURIZING SUNSCREEN drug offered from Rodial, 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: Rodial, Ltd.
NON-PROPRIETARY NAME: HOMOSALATE, OCTINOXATE, OXYBENZONE
SUBSTANCE NAME: HOMOSALATE; OCTINOXATE; OXYBENZONE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: LIQUID
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2010-06-30
END MARKETING DATE: 0000-00-00


GLAMTOX ACTIVE DAILY MOISTURIZING SUNSCREEN HUMAN OTC DRUG Details:

Item DescriptionGLAMTOX ACTIVE DAILY MOISTURIZING SUNSCREEN from Rodial, Ltd.
LABELER NAME: Rodial, Ltd.
DEA SCHEDULE:
ACTIVE STRENGTH: 3; 8; 2(mL/100mL; mL/100mL; mL/100mL)
START MARKETING DATE: 2010-06-30
END MARKETING DATE: 0000-00-00
PRODUCT ID: 52456-018_05a1089e-1936-4921-a7df-4beffe53f454
PRODUCT NDC: 52456-018
APPLICATION NUMBER: part352

Other HOMOSALATE; OCTINOXATE; OXYBENZONE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Mary Kay Inc.Mary Kay CC Cream Sunscreen Broad Spectrum SPF 15 Very Light
Rodial, Ltd.GLAMTOX ACTIVE DAILY MOISTURIZING SUNSCREEN