T-RELIEF PRO ARTHRITIS- arnica montana, bryonia alba whole, sus scrofa cartilage,solanum dulcamara top,sus scrofa embryo,sus scrofa umbilical cord,rhododendron tomentosum leafy twig,sus scrofa placenta,rhododendron aureum leaf,toxicodendron pubescens leaf, sanguinaria canadensis root, sulfur and comfrey root tablet

T-Relief PRO Arthritis by

Drug Labeling and Warnings

T-Relief PRO Arthritis by is a Homeopathic medication manufactured, distributed, or labeled by MediNatura Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

WARNINGS

Do not use If pregnant or breast-feeding. Keep out of reach of children. If symptoms persist or worsen, a health professional should be consulted. Do not use if known sensitivity to T-Relief Arthritis or any of its ingredients exists.

INGREDIENTS

Arnica montana 3X 5%, Bryonia alba 3X 0.15%, Bryonia alba 6X 0.15%, Bryonia alba 12X 0.15% mg., Cartilago suis 4X 0.15%, Dulcamara 2X 2.5%, Embryo suis 6X 0.15%, Funiculus umbilicalis suis 6X 0.15%, Ledum palustre 6X 2%, Placenta lolasis suis 6X 0.15%, Rhododendron chrysanthum 8X 0.15%, Rhus toxicodendron 4X 2.5%, Sanguinaria canadensis 3X 0.25%, Sulphur 6X 2.5%, . Symphytum officinale 7X 0.01%.

USES

Arthritis Pain relief tablets
Supports Mobility
Joint Stiffness
Arthritis Pain
Joint Pain

INACTIVE INGREDIENT

Lactose, Magnesium stearate

INDICATIONS

For the temporary relief of minor Joint Stiffness, Arthritis Pain, Joint Pain.

DIRECTIONS

Adults : Chew 2 tablet every 4 hours or as directed by health professional. For Children under 18 years, use as directed by health professional

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

T-RELIEF PRO ARTHRITIS 
arnica montana, bryonia alba whole, sus scrofa cartilage,solanum dulcamara top,sus scrofa embryo,sus scrofa umbilical cord,rhododendron tomentosum leafy twig,sus scrofa placenta,rhododendron aureum leaf,toxicodendron pubescens leaf, sanguinaria canadensis root, sulfur and comfrey root tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62795-1039
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW)	ARNICA MONTANA	3 [hp_X]
BRYONIA ALBA WHOLE (UNII: 56K0VVT47P) (BRYONIA ALBA WHOLE - UNII:56K0VVT47P)	BRYONIA ALBA WHOLE	3 [hp_X]
SUS SCROFA CARTILAGE (UNII: 73ECW5WG2F) (SUS SCROFA CARTILAGE - UNII:73ECW5WG2F)	SUS SCROFA CARTILAGE	4 [hp_X]
SOLANUM DULCAMARA TOP (UNII: KPS1B1162N) (SOLANUM DULCAMARA TOP - UNII:KPS1B1162N)	SOLANUM DULCAMARA TOP	2 [hp_X]
SUS SCROFA EMBRYO (UNII: 9928MC12VO) (SUS SCROFA EMBRYO - UNII:9928MC12VO)	SUS SCROFA EMBRYO	6 [hp_X]
SUS SCROFA UMBILICAL CORD (UNII: 118OYG6W3H) (SUS SCROFA UMBILICAL CORD - UNII:118OYG6W3H)	SUS SCROFA UMBILICAL CORD	6 [hp_X]
RHODODENDRON TOMENTOSUM LEAFY TWIG (UNII: 877L01IZ0P) (LEDUM PALUSTRE TWIG - UNII:877L01IZ0P)	RHODODENDRON TOMENTOSUM LEAFY TWIG	6 [hp_X]
SUS SCROFA PLACENTA (UNII: C8CV8867O8) (SUS SCROFA PLACENTA - UNII:C8CV8867O8)	SUS SCROFA PLACENTA	6 [hp_X]
RHODODENDRON AUREUM LEAF (UNII: IV92NQJ73U) (RHODODENDRON AUREUM LEAF - UNII:IV92NQJ73U)	RHODODENDRON AUREUM LEAF	8 [hp_X]
TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A)	TOXICODENDRON PUBESCENS LEAF	4 [hp_X]
SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (SANGUINARIA CANADENSIS ROOT - UNII:N9288CD508)	SANGUINARIA CANADENSIS ROOT	3 [hp_X]
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	6 [hp_X]
COMFREY ROOT (UNII: M9VVZ08EKQ) (COMFREY ROOT - UNII:M9VVZ08EKQ)	COMFREY ROOT	7 [hp_X]

Inactive Ingredients
Ingredient Name	Strength
LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)
MAGNESIUM STEARATE (UNII: 70097M6I30)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	9mm
Flavor		Imprint Code	Leafman
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62795-1039-2	100 in 1 PACKAGE; Type 0: Not a Combination Product	12/13/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		12/13/2017

Labeler - MediNatura Inc (079324099)

Establishment
Name	Address	ID/FEI	Business Operations
MediNatura Inc		102783016	manufacture(62795-1039)