GUNA-AWARENESS (Guna spa)


Welcome to the PulseAid listing for the GUNA-AWARENESS 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: BETAINE – BUFO BUFO CUTANEOUS GLAND – CALCIUM CARBONATE – CHROMIC SULFATE – CICUTA VIROSA ROOT – COPPER – FOLIC ACID – GOLD – COBALAMIN – IRON – LACHESIS MUTA VENOM – MELATONIN – MOLYBDENUM – NEUROTRO
SUBSTANCE NAME: GOLD; BRAIN-DERIVED NEUROTROPHIC FACTOR HUMAN; BUFO BUFO CUTANEOUS GLAND; CALCIUM CARBONATE; CHROMIC SULFATE; CICUTA VIROSA ROOT; COBALAMIN; UBIDECARENONE; COPPER; IRON; FOLIC ACID; SUS SCROFA FRONTAL
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: SOLUTION/ DROPS
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2008-04-16
END MARKETING DATE: 0000-00-00


GUNA-AWARENESS HUMAN OTC DRUG Details:

Item DescriptionGUNA-AWARENESS from Guna spa
LABELER NAME: Guna spa
DEA SCHEDULE:
ACTIVE STRENGTH: 12; 4; 12; 3; 3; 12; 3; 3; 12; 3; 3; 6; 12; 4; 3; 4; 4; 6; 12; 6; 3; 3; 6; 3([hp_X]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_C)
START MARKETING DATE: 2008-04-16
END MARKETING DATE: 0000-00-00
PRODUCT ID: 17089-350_29d041d6-96e1-4c0d-a94d-33618467c63d
PRODUCT NDC: 17089-350
APPLICATION NUMBER:

Other GOLD; BRAIN-DERIVED NEUROTROPHIC FACTOR HUMAN; BUFO BUFO CUTANEOUS GLAND; CALCIUM CARBONATE; CHROMIC SULFATE; CICUTA VIROSA ROOT; COBALAMIN; UBIDECARENONE; COPPER; IRON; FOLIC ACID; SUS SCROFA FRONTAL Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Guna spaGUNA-AWARENESS