BABY ECZEMA RELIEF (PUREMEDY)


Welcome to the PulseAid listing for the BABY ECZEMA RELIEF drug offered from PUREMEDY. 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: PUREMEDY
NON-PROPRIETARY NAME: CALENDULA OFFICINALIS FLOWER, SAMBUCUS NIGRA FLOWER
SUBSTANCE NAME: CALENDULA OFFICINALIS FLOWER; SAMBUCUS NIGRA FLOWER
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: SALVE
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2012-10-18
END MARKETING DATE: 0000-00-00


BABY ECZEMA RELIEF HUMAN OTC DRUG Details:

Item DescriptionBABY ECZEMA RELIEF from PUREMEDY
LABELER NAME: PUREMEDY
DEA SCHEDULE:
ACTIVE STRENGTH: 1; 1([hp_X]/100mL; [hp_X]/100mL)
START MARKETING DATE: 2012-10-18
END MARKETING DATE: 0000-00-00
PRODUCT ID: 52810-217_f29107e4-0896-4075-96e2-298a5762e3bf
PRODUCT NDC: 52810-217
APPLICATION NUMBER:

Other CALENDULA OFFICINALIS FLOWER; SAMBUCUS NIGRA FLOWER Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
PUREMEDYBABY ECZEMA RELIEF