Dr G Whitening REFORMER by EGF (The Doctor’s Cosmetic Inc)


Welcome to the PulseAid listing for the Dr G Whitening REFORMER by EGF drug offered from The Doctor’s Cosmetic 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: The Doctor’s Cosmetic Inc
NON-PROPRIETARY NAME: ARBUTIN DIMETHICONE
SUBSTANCE NAME: ARBUTIN; DIMETHICONE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: CREAM
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2009-11-01
END MARKETING DATE: 0000-00-00


Dr G Whitening REFORMER by EGF HUMAN OTC DRUG Details:

Item DescriptionDr G Whitening REFORMER by EGF from The Doctor’s Cosmetic Inc
LABELER NAME: The Doctor’s Cosmetic Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 1; 2(mL/50mL; mL/50mL)
START MARKETING DATE: 2009-11-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 43948-4002_d9290e62-272d-417d-880d-ab29790125d2
PRODUCT NDC: 43948-4002
APPLICATION NUMBER: part347

Other ARBUTIN; DIMETHICONE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
The Doctor’s Cosmetic IncDr G Whitening REFORMER by EGF