VANOXIDEHC (Summers Laboratories Inc)


Welcome to the PulseAid listing for the VANOXIDE drug offered from Summers Laboratories Inc. This Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [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: Summers Laboratories Inc
NON-PROPRIETARY NAME: BENZOYL PEROXIDE, HYDROCORTISONE
SUBSTANCE NAME: BENZOYL PEROXIDE; HYDROCORTISONE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
ROUTE: TOPICAL
DOSAGE FORM: LOTION
MARKETING CATEGORY NAME: UNAPPROVED DRUG OTHER
START MARKETING DATE: 2009-11-01
END MARKETING DATE: 0000-00-00


VANOXIDE HC HUMAN PRESCRIPTION DRUG Details:

Item DescriptionVANOXIDE HC from Summers Laboratories Inc
LABELER NAME: Summers Laboratories Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 5; .5(g/100g; g/100g)
START MARKETING DATE: 2009-11-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 11086-032_c0de33e9-17c1-43e2-8859-2805e821c81e
PRODUCT NDC: 11086-032
APPLICATION NUMBER:

Other BENZOYL PEROXIDE; HYDROCORTISONE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Summers Laboratories IncVANOXIDE