DR. HENDEL ARTHRITIS PAIN RELIEF- bryonia alba root, arnica montana, colchicum autumnale bulb, solanum dulcamara top, harpagophytum procumbens root, ledum palustre twig, rhododendron aureum leaf,comfrey root, toxicodendron pubescens leaf, oyster shell calcium carbonate, crude, tribasic calcium phosphate, and silicon dioxide tablet

Dr. Hendel Arthritis Pain Relief by

Drug Labeling and Warnings

Dr. Hendel Arthritis Pain Relief by is a Homeopathic medication manufactured, distributed, or labeled by MediNatura Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

WARNINGS

If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If symptoms persist or

worsen, a health professional should be consulted. Do not use if sensitivity to Hendel Arthritis Pain Relief or any of its ingredients exists. In case of accidental overdose, contact a Poison Control Center immediately.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

INDICATIONS

Arthritis Pain Relief

ACTIVE INGREDIENT

Each tablet containsequal parts of: Bryonia 4X; Arnica montana 6X; Colchicum autumnale 6X; Dulcamara 6X; Harpagophytum 6X; Ledum palustre 6X; Rhododendron chrysanthum 6X; Symphytum officinale 6X; Rhus tox 8X, 12X, 30X; Calcarea carbonica 12X, Calcarea phosphorica 12X; Silicea 12X

INACTIVE INGREDIENT

Lactose, Magnesium stearate

DIRECTIONS

Dosage: Adults 18 and over: 1 tablet sublingually or dissolved completely in mouth 2 to 3 times per day or as directed by a physician.

USES

For the temporary relief of:

Bone & joint pain

Aching muscles

Dr. Hendel Arthritis Pain Relief

INGREDIENTS AND APPEARANCE

DR. HENDEL ARTHRITIS PAIN RELIEF 
bryonia alba root, arnica montana, colchicum autumnale bulb, solanum dulcamara top, harpagophytum procumbens root, ledum palustre twig, rhododendron aureum leaf,comfrey root, toxicodendron pubescens leaf, oyster shell calcium carbonate, crude, tribasic calcium phosphate, and silicon dioxide tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62795-1113
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B)	BRYONIA ALBA ROOT	4 [hp_X]
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW)	ARNICA MONTANA	6 [hp_X]
COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6) (COLCHICUM AUTUMNALE BULB - UNII:993QHL78E6)	COLCHICUM AUTUMNALE BULB	6 [hp_X]
SOLANUM DULCAMARA TOP (UNII: KPS1B1162N) (SOLANUM DULCAMARA TOP - UNII:KPS1B1162N)	SOLANUM DULCAMARA TOP	6 [hp_X]
HARPAGOPHYTUM PROCUMBENS ROOT (UNII: 1OYM338E89) (HARPAGOPHYTUM PROCUMBENS ROOT - UNII:1OYM338E89)	HARPAGOPHYTUM PROCUMBENS ROOT	6 [hp_X]
LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P) (LEDUM PALUSTRE TWIG - UNII:877L01IZ0P)	LEDUM PALUSTRE TWIG	6 [hp_X]
RHODODENDRON AUREUM LEAF (UNII: IV92NQJ73U) (RHODODENDRON AUREUM LEAF - UNII:IV92NQJ73U)	RHODODENDRON AUREUM LEAF	6 [hp_X]
COMFREY ROOT (UNII: M9VVZ08EKQ) (COMFREY ROOT - UNII:M9VVZ08EKQ)	COMFREY ROOT	6 [hp_X]
TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A)	TOXICODENDRON PUBESCENS LEAF	8 [hp_X]
OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I)	OYSTER SHELL CALCIUM CARBONATE, CRUDE	12 [hp_X]
TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM CATION	12 [hp_X]
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	3 [hp_X]

Inactive Ingredients
Ingredient Name	Strength
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
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: 62795-1113-2	100 in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		08/01/2016

Labeler - MediNatura Inc (079324099)

Establishment
Name	Address	ID/FEI	Business Operations
MediNatura Inc		102783016	manufacture(62795-1113)