GUNA-COUGH (Guna spa)


Welcome to the PulseAid listing for the GUNA-COUGH drug offered from Guna spa. 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: Guna spa
NON-PROPRIETARY NAME: ALTHAEA OFFICINALIS LEAF – ANTIMONY POTASSIUM TARTRATE – BRYONIA ALBA ROOT – CETRARIA ISLANDICA SUBSP. ISLANDICA – COCHINEAL – COPPER – DROSERA ROTUNDIFOLIA – ECHINACEA ANGUSTIFOLIA – GARDEN THYME – L
SUBSTANCE NAME: ALTHAEA OFFICINALIS LEAF; ANTIMONY POTASSIUM TARTRATE; BRYONIA ALBA ROOT; CETRARIA ISLANDICA SUBSP. ISLANDICA; COCHINEAL; COPPER; DROSERA ROTUNDIFOLIA; ECHINACEA ANGUSTIFOLIA; PLANTAGO MAJOR; LOBARIA
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: SOLUTION/ DROPS
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2010-05-27
END MARKETING DATE: 0000-00-00


GUNA-COUGH HUMAN OTC DRUG Details:

Item DescriptionGUNA-COUGH from Guna spa
LABELER NAME: Guna spa
DEA SCHEDULE:
ACTIVE STRENGTH: 1; 8; 6; 4; 6; 8; 1; 1; 1; 4; 1([hp_X]/150mL; [hp_X]/150mL; [hp_X]/150mL; [hp_X]/150mL; [hp_X]/150mL; [hp_X]/150mL; [hp_X]/150mL; [hp_X]/150mL; [hp_X]/150mL; [hp_X]/150mL; [hp_X]/150mL)
START MARKETING DATE: 2010-05-27
END MARKETING DATE: 0000-00-00
PRODUCT ID: 17089-453_954bfe17-6d04-4ed2-9a37-a212517107eb
PRODUCT NDC: 17089-453
APPLICATION NUMBER:

Other ALTHAEA OFFICINALIS LEAF; ANTIMONY POTASSIUM TARTRATE; BRYONIA ALBA ROOT; CETRARIA ISLANDICA SUBSP. ISLANDICA; COCHINEAL; COPPER; DROSERA ROTUNDIFOLIA; ECHINACEA ANGUSTIFOLIA; PLANTAGO MAJOR; LOBARIA Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Guna spaGUNA-COUGH