TinnitusDX (Apotheca Company)


Welcome to the PulseAid listing for the Tinnitus drug offered from Apotheca Company. 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: Apotheca Company
NON-PROPRIETARY NAME: Calcarea carbonica, Carbo vegetabilis, Chininum sulphuricum, Cimicifuga racemosa, Cinchona officinalis, Coffea cruda, Graphites, Kali carbonicum,
SUBSTANCE NAME: OYSTER SHELL CALCIUM CARBONATE, CRUDE; ACTIVATED CHARCOAL; QUININE SULFATE; BLACK COHOSH; CINCHONA OFFICINALIS BARK; ARABICA COFFEE BEAN; GRAPHITE; POTASSIUM CARBONATE; LYCOPODIUM CLAVATUM SPORE; SODI
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: CAPSULE
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2010-11-12
END MARKETING DATE: 0000-00-00


Tinnitus DX HUMAN OTC DRUG Details:

Item DescriptionTinnitus DX from Apotheca Company
LABELER NAME: Apotheca Company
DEA SCHEDULE:
ACTIVE STRENGTH: 30; 30; 30; 30; 30; 12; 30; 30; 30; 6; 6([hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1)
START MARKETING DATE: 2010-11-12
END MARKETING DATE: 0000-00-00
PRODUCT ID: 57520-0363_a2b4738b-db33-4f58-80b6-e5fc163f3043
PRODUCT NDC: 57520-0363
APPLICATION NUMBER:

Other OYSTER SHELL CALCIUM CARBONATE, CRUDE; ACTIVATED CHARCOAL; QUININE SULFATE; BLACK COHOSH; CINCHONA OFFICINALIS BARK; ARABICA COFFEE BEAN; GRAPHITE; POTASSIUM CARBONATE; LYCOPODIUM CLAVATUM SPORE; SODI Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Apotheca CompanyTinnitus