NDC 68703-104

TMJ Ease

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 Ease is a Oral Spray in the Human Otc Drug category. It is labeled and distributed by Native Remedies, Llc. 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 ID: 68703-104_f8398470-313b-4c72-abcd-4b6c833f70ad
• NDC: 68703-104
• Product Type: Human Otc Drug
• Proprietary Name: TMJ Ease
• Generic Name: Baptisia Tinctoria, Calcarea Fluorica, Causticum, Hepar Sulphuris Calcareum, Hypericum Perforatum, Ignatia Amara, Kalmia Latifolia, Nux Vomica, Phytolacca Decandra, Rhus Toxicodendron, Sanguinaria Canadensis, Symphytum Officinale
• Dosage Form: Spray
• Route of Administration: ORAL
• Marketing Start Date: 2013-06-27
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Native Remedies, LLC
• Substance Name: 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
• Active Ingredient Strength: 10 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; 1/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 68703-104-59

59 mL in 1 BOTTLE, GLASS (68703-104-59)

• Marketing Start Date: 2013-06-27
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 68703-104-59 [68703010459]

TMJ Ease SPRAY

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-06-27
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
BAPTISIA TINCTORIA ROOT	10 [hp_X]/59mL

OpenFDA Data

• SPL SET ID: 4f6e4ad1-3992-4d1b-9505-23d98e63ce32
• Manufacturer:
  • Native Remedies, LLC
• UNII:
  • N9288CD508
  • O3B55K4YKI
  • 5EF0HWI5WU
  • 6IO182RP7A
  • M9VVZ08EKQ
  • DD5FO1WKFU
  • 79N6542N18
  • 11E6VI8VEG
  • XK4IUX8MNB
  • 1MBW07J51Q
  • 1NM3M2487K
  • 269XH13919
• UPC Code:
  • 0818837010402