Bone Repair

Product NDC

44911-0067

11-digit product format

449110067

Labeler code

44911

Product ID

44911-0067_2a03a69e-d487-49ee-91c6-d4c7afcde6bf

Type

HUMAN OTC DRUG

Nonproprietary name

Calcarea Carbonica, Calcarea Fluorica, Calcarea Phosphorica, Hekla Lava, Hydrofluoricum Acidum, Magnesia Phosphorica, Rhus Tox, Ruta Graveolens, Silicea, Symphytum Officinale

Dosage form

LIQUID

Route

ORAL

Labeler

Energique, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2013-02-20

Marketing end

2023-12-10

Substance

CALCIUM FLUORIDE; COMFREY ROOT; HEKLA LAVA; HYDROFLUORIC ACID; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; RUTA GRAVEOLENS FLOWERING TOP; SILICON DIOXIDE; TOXICODENDRON PUBESCENS LEAF; TRIBASIC CALCIUM PHOSPHATE

Active strength

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

Pharmacologic classes

Blood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record