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Arthritis Joints

FULL PRESCRIBING INFORMATION

Active ingredient

ACTIVE INGREDIENTS: Gnaphalium polycephalum 3X, Berberis vulgaris 4X, Cimicifuga racemosa 4X, Cinchona officinalis 4X, Colocynthis 4X, Ledum palustre 4X, Ranunculus bulbosus 4X, Aesculus hippocastanum 6X, Borax 6X, Cuprum aceticum 6X, Kali carbonicum 6X, Pulsatilla 6X, Secale cornutum 6X, Ammonium muriaticum 8X, Silicea 8X, Argentum metallicum 10X, Calcarea phosphorica 10X, Glandula suprarenalis suis 10X, Mercurius praecipitatus ruber 10X, Sepia 10X, Zincum metallicum 10X, Palladium metallicum 12X, Picricum acidum 12X, Sulphur 30X, Cartilago suis 12C, Intervertebral disc suis 12C, Medulla ossis suis 12C.

Purpose

INDICATIONS: For temporary relief of symptoms related to arthritis, osteoporosis, rheumatism and neuralgia including rash, itching, numbness and tingling, stress and anxiety, headache, fatigue, swelling, and joint pain.

WARNINGS: Keep out of reach of children. In case of overdose, contact physician or Poison Control Center right away.

If pregnant or breast-feeding, seek advice of a health professional before use.

Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.

DIRECTIONS: 1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

INACTIVE INGREDIENTS: Demineralized water, 25% Ethanol.

KEEP OUT OF REACH OF CHILDREN. In case of overdose, contact physician or Poison Control Center right away.

Uses

Dist. By: Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84070

www.desbio.com

DESBIO

NDC 57520-0925-1

HOMEOPATHIC

ARTHRITIS JOINTS

1 FL OZ (30 ml)

Arthritis Joints

Gnaphalium polycephalum, Berberis vulgaris, Cimicifuga racemosa, Cinchona officinalis, Colocynthis, Ledum palustre, Ranunculus bulbosus, Aesculus hippocastanum, Borax, Cuprum aceticum, Kali carbonicum, Pulsatilla, Secale cornutum, LIQUID

Product Information
Product Type	Human otc drug label	Item Code (Source)	NDC:57520-0925
Route of Administration	ORAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PSEUDOGNAPHALIUM OBTUSIFOLIUM PSEUDOGNAPHALIUM OBTUSIFOLIUM		3 [hp_X]
BERBERIS VULGARIS ROOT BARK BERBERIS VULGARIS ROOT BARK		4 [hp_X]
BLACK COHOSH BLACK COHOSH		4 [hp_X]
Cinchona Officinalis Bark Cinchona Officinalis Bark		4 [hp_X]
CITRULLUS COLOCYNTHIS FRUIT PULP CITRULLUS COLOCYNTHIS FRUIT PULP		4 [hp_X]
LEDUM PALUSTRE TWIG LEDUM PALUSTRE TWIG		4 [hp_X]
Ranunculus Bulbosus Ranunculus Bulbosus		4 [hp_X]
HORSE CHESTNUT HORSE CHESTNUT		6 [hp_X]
SODIUM BORATE		6 [hp_X]
CUPRIC ACETATE CUPRIC CATION		6 [hp_X]
POTASSIUM CARBONATE CARBONATE ION		6 [hp_X]
PULSATILLA VULGARIS PULSATILLA VULGARIS		6 [hp_X]
CLAVICEPS PURPUREA SCLEROTIUM CLAVICEPS PURPUREA SCLEROTIUM		6 [hp_X]
AMMONIUM CHLORIDE AMMONIUM CATION		8 [hp_X]
SILICON DIOXIDE		8 [hp_X]
SILVER Silver		10 [hp_X]
TRIBASIC CALCIUM PHOSPHATE CALCIUM CATION		10 [hp_X]
SUS SCROFA ADRENAL GLAND SUS SCROFA ADRENAL GLAND		10 [hp_X]
MERCURIC OXIDE, YELLOW MERCURIC OXIDE, YELLOW		10 [hp_X]
SEPIA OFFICINALIS JUICE SEPIA OFFICINALIS JUICE		10 [hp_X]
Zinc ZINC		10 [hp_X]
PALLADIUM PALLADIUM		12 [hp_X]
TRINITROPHENOL TRINITROPHENOL		12 [hp_X]
SULFUR SULFUR		30 [hp_X]
SUS SCROFA CARTILAGE Sus Scrofa Cartilage		12 [hp_C]
SUS SCROFA INTERVERTEBRAL DISC SUS SCROFA INTERVERTEBRAL DISC		12 [hp_C]
SUS SCROFA BONE MARROW SUS SCROFA BONE MARROW		12 [hp_C]

Inactive Ingredients
Ingredient Name	Strength
water
ALCOHOL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC:57520-0925-1	30 in 1 BOTTLE, DROPPER

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
		2011-10-24

PLEASE, BE CAREFUL!

Be sure to consult your doctor before taking any medication!