Natralia Anti-Itch Soothing (LaCorium Health USA Inc)


Welcome to the PulseAid listing for the Natralia Anti-Itch Soothing drug offered from LaCorium Health 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: LaCorium Health USA Inc
NON-PROPRIETARY NAME: OATMEAL and Menthol
SUBSTANCE NAME: OATMEAL; MENTHOL, UNSPECIFIED FORM
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: CREAM
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2013-01-10
END MARKETING DATE: 0000-00-00


Natralia Anti-Itch Soothing HUMAN OTC DRUG Details:

Item DescriptionNatralia Anti-Itch Soothing from LaCorium Health USA Inc
LABELER NAME: LaCorium Health USA Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 20; 6(mg/g; mg/g)
START MARKETING DATE: 2013-01-10
END MARKETING DATE: 0000-00-00
PRODUCT ID: 43251-3345_e0ac2feb-c135-41da-8501-b7c85d5c5e9c
PRODUCT NDC: 43251-3345
APPLICATION NUMBER: part347

Other OATMEAL; MENTHOL, UNSPECIFIED FORM Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
LaCorium Health USA IncNatralia Anti-Itch Soothing