Kali Sulf. Bath Essence (Uriel Pharmacy Inc.)


Welcome to the PulseAid listing for the Kali Sulf. Bath Essence drug offered from Uriel Pharmacy 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: Uriel Pharmacy Inc.
NON-PROPRIETARY NAME: Kali Sulf. Bath Essence
SUBSTANCE NAME: POTASSIUM SULFIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: LIQUID
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2009-09-01
END MARKETING DATE: 0000-00-00


Kali Sulf. Bath Essence HUMAN OTC DRUG Details:

Item DescriptionKali Sulf. Bath Essence from Uriel Pharmacy Inc.
LABELER NAME: Uriel Pharmacy Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 1([hp_X]/mL)
START MARKETING DATE: 2009-09-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 48951-6005_e3cafac5-b3cb-4454-8237-c0af3d9bd2e3
PRODUCT NDC: 48951-6005
APPLICATION NUMBER:

Other POTASSIUM SULFIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Uriel Pharmacy Inc.Kali Sulf. Bath Essence