Spascupreel (Heel Inc)


Welcome to the PulseAid listing for the Spascupreel drug offered from Heel 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: Heel Inc
NON-PROPRIETARY NAME: ACONITUM NAPELLUS and AMMONIUM BROMIDE and CITRULLUS COLOCYNTHIS FRUIT PULP and ATROPINE SULFATE and GELSEMIUM SEMPERVIRENS ROOT and MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE and VERATRUM ALBUM ROOT and
SUBSTANCE NAME: ACONITUM NAPELLUS; AMMONIUM BROMIDE; CITRULLUS COLOCYNTHIS FRUIT PULP; ATROPINE SULFATE; GELSEMIUM SEMPERVIRENS ROOT; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; VERATRUM ALBUM ROOT; PASSIFLORA INCARNATA
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: SOLUTION
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 1993-01-31
END MARKETING DATE: 0000-00-00


Spascupreel HUMAN OTC DRUG Details:

Item DescriptionSpascupreel from Heel Inc
LABELER NAME: Heel Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 6; 4; 4; 6; 6; 6; 6; 2; 3; 4; 6([hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL)
START MARKETING DATE: 1993-01-31
END MARKETING DATE: 0000-00-00
PRODUCT ID: 50114-6129_eab7b089-635c-472d-a952-8ad4f063ae0c
PRODUCT NDC: 50114-6129
APPLICATION NUMBER:

Other ACONITUM NAPELLUS; AMMONIUM BROMIDE; CITRULLUS COLOCYNTHIS FRUIT PULP; ATROPINE SULFATE; GELSEMIUM SEMPERVIRENS ROOT; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; VERATRUM ALBUM ROOT; PASSIFLORA INCARNATA Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Heel IncSpascupreel
MediNatura IncSpascupreel