NDC 57955-5032

TMJ / Jaw Formula

Baptisia Tinctoria, Calcarea Fluorica, Causticum, Hepar Sulphuris Calcareum, Hypericum Perforatum, Ignatia Amara, Kalmia Latifolia, Nux Vomica, Phytolacca Decandra, Rhus Toxicodendron Sanguinaria Canadensis, Symphytum Officinale

TMJ / Jaw Formula is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by King Bio Inc.. The primary component is Baptisia Tinctoria Root; Calcium Fluoride; Causticum; Calcium Sulfide; Hypericum Perforatum; Strychnos Ignatii Seed; Kalmia Latifolia Leaf; Strychnos Nux-vomica Seed; Phytolacca Americana Root; Toxicodendron Pubescens Leaf; Sanguinaria Canadensis Root; Comfrey Root.

Product ID57955-5032_ffbecae3-dbd5-4a51-a043-81502c499b9b
NDC57955-5032
Product TypeHuman Otc Drug
Proprietary NameTMJ / Jaw Formula
Generic NameBaptisia Tinctoria, Calcarea Fluorica, Causticum, Hepar Sulphuris Calcareum, Hypericum Perforatum, Ignatia Amara, Kalmia Latifolia, Nux Vomica, Phytolacca Decandra, Rhus Toxicodendron Sanguinaria Canadensis, Symphytum Officinale
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2016-03-18
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameKing Bio Inc.
Substance NameBAPTISIA TINCTORIA ROOT; CALCIUM FLUORIDE; CAUSTICUM; CALCIUM SULFIDE; HYPERICUM PERFORATUM; STRYCHNOS IGNATII SEED; KALMIA LATIFOLIA LEAF; STRYCHNOS NUX-VOMICA SEED; PHYTOLACCA AMERICANA ROOT; TOXICODENDRON PUBESCENS LEAF; SANGUINARIA CANADENSIS ROOT; COMFREY ROOT
Active Ingredient Strength10 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 57955-5032-2

59 mL in 1 BOTTLE, SPRAY (57955-5032-2)
Marketing Start Date2016-03-18
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 57955-5032-2 [57955503202]

TMJ / Jaw Formula LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-03-18
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
BAPTISIA TINCTORIA ROOT10 [hp_X]/59mL

OpenFDA Data

SPL SET ID:228fe129-67c8-4003-97dd-801ec3fd8518
Manufacturer
UNII

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