Bone RepairHP (Energique, Inc.)


Welcome to the PulseAid listing for the Bone Repair 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: Calcarea Carbonica, Calcarea Fluorica, Calcarea Phosphorica, Hekla Lava, Hydrofluoricum Acidum, Magnesia Phosphorica, Rhus Tox, Ruta Graveolens, Silicea, Symphytum Officinale
SUBSTANCE NAME: OYSTER SHELL CALCIUM CARBONATE, CRUDE; CALCIUM FLUORIDE; TRIBASIC CALCIUM PHOSPHATE; HEKLA LAVA; HYDROFLUORIC ACID; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; TOXICODENDRON PUBESCENS LEAF; RUTA GRAVEOLE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: LIQUID
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2013-02-20
END MARKETING DATE: 0000-00-00


Bone Repair HP HUMAN OTC DRUG Details:

Item DescriptionBone Repair HP from Energique, Inc.
LABELER NAME: Energique, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 30; 30; 30; 30; 30; 30; 30; 30; 30; 30([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; [hp_X]/mL)
START MARKETING DATE: 2013-02-20
END MARKETING DATE: 0000-00-00
PRODUCT ID: 44911-0067_a51a42c5-104c-40f7-bf55-ac4ebc011c2e
PRODUCT NDC: 44911-0067
APPLICATION NUMBER:

Other OYSTER SHELL CALCIUM CARBONATE, CRUDE; CALCIUM FLUORIDE; TRIBASIC CALCIUM PHOSPHATE; HEKLA LAVA; HYDROFLUORIC ACID; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; TOXICODENDRON PUBESCENS LEAF; RUTA GRAVEOLE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Apotheca CompanyBone Repair
Energique, Inc.Bone Repair