TEETHING KIDS RELIEF (HOMEOLAB USA INC)


Welcome to the PulseAid listing for the TEETHING KIDS RELIEF drug offered from HOMEOLAB 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: HOMEOLAB USA INC
NON-PROPRIETARY NAME: CHAMOMILLA, ARNICA MONTANA, BORAX, HYPERICUM PERFORATUM
SUBSTANCE NAME: MATRICARIA RECUTITA; ARNICA MONTANA; SODIUM BORATE; HYPERICUM PERFORATUM
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: LIQUID
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2008-08-18
END MARKETING DATE: 0000-00-00


TEETHING KIDS RELIEF HUMAN OTC DRUG Details:

Item DescriptionTEETHING KIDS RELIEF from HOMEOLAB USA INC
LABELER NAME: HOMEOLAB USA INC
DEA SCHEDULE:
ACTIVE STRENGTH: 5; 5; 5; 5([hp_C]/25mL; [hp_C]/25mL; [hp_C]/25mL; [hp_C]/25mL)
START MARKETING DATE: 2008-08-18
END MARKETING DATE: 0000-00-00
PRODUCT ID: 60512-9060_7fc50292-4009-4941-b5e0-29e05f03f92c
PRODUCT NDC: 60512-9060
APPLICATION NUMBER:

Other MATRICARIA RECUTITA; ARNICA MONTANA; SODIUM BORATE; HYPERICUM PERFORATUM Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
CVS PHARMACYTEETHING
HOMEOLAB USA INCTEETHING KIDS RELIEF