Acnetone (Energique, Inc.)


Welcome to the PulseAid listing for the Acnetone drug offered from Energique, 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: Energique, Inc.
NON-PROPRIETARY NAME: Berberis Vulgaris, Cimicifuga Racemosa, Antimonium Crudum, Carbo Vegetabilis, Hepar Sulphuris Calcareum, Kali Iodatum, Lycopodium Clavatum, Sepia, Sulphur
SUBSTANCE NAME: BERBERIS VULGARIS ROOT BARK; BLACK COHOSH; ANTIMONY TRISULFIDE; ACTIVATED CHARCOAL; CALCIUM SULFIDE; POTASSIUM IODIDE; LYCOPODIUM CLAVATUM SPORE; SEPIA OFFICINALIS JUICE; SULFUR
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: LIQUID
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2016-03-30
END MARKETING DATE: 0000-00-00


Acnetone HUMAN OTC DRUG Details:

Item DescriptionAcnetone from Energique, Inc.
LABELER NAME: Energique, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 3; 3; 12; 12; 12; 12; 12; 12; 12([hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL)
START MARKETING DATE: 2016-03-30
END MARKETING DATE: 0000-00-00
PRODUCT ID: 44911-0337_08d6a818-3758-4a9b-b847-62fe183a6e07
PRODUCT NDC: 44911-0337
APPLICATION NUMBER:

Other BERBERIS VULGARIS ROOT BARK; BLACK COHOSH; ANTIMONY TRISULFIDE; ACTIVATED CHARCOAL; CALCIUM SULFIDE; POTASSIUM IODIDE; LYCOPODIUM CLAVATUM SPORE; SEPIA OFFICINALIS JUICE; SULFUR Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Energique, Inc.Acnetone