UNDA MOSITURIZING (UNDA)


Welcome to the PulseAid listing for the UNDA MOSITURIZING drug offered from UNDA. 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: UNDA
NON-PROPRIETARY NAME: Salicylic Acid, Bambusa Vulgaris Extract, Eucalyptus Globulus Leaf Oil
SUBSTANCE NAME: SALICYLIC ACID; EUCALYPTUS GLOBULUS LEAF; BAMBUSA VULGARIS TOP
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: SHAMPOO
MARKETING CATEGORY NAME: UNAPPROVED DRUG OTHER
START MARKETING DATE: 2016-07-01
END MARKETING DATE: 0000-00-00


UNDA MOSITURIZING HUMAN OTC DRUG Details:

Item DescriptionUNDA MOSITURIZING from UNDA
LABELER NAME: UNDA
DEA SCHEDULE:
ACTIVE STRENGTH: .001; .1; 53.13(g/100mL; g/100mL; g/100mL)
START MARKETING DATE: 2016-07-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 70845-0011_386db1d4-3da6-223b-e054-00144ff8d46c
PRODUCT NDC: 70845-0011
APPLICATION NUMBER:

Other SALICYLIC ACID; EUCALYPTUS GLOBULUS LEAF; BAMBUSA VULGARIS TOP Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
UNDAUNDA MOSITURIZING