BHI Arthritis description, usages, side effects, indications, overdosage, supplying and lots more!

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BHI Arthritis

Heel Inc

BHI Arthritis


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

KEEP OUT OF REACH OF CHILDREN

Keep this and all medicines out of the reach of children.

WARNINGS

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

BHI ARTHRITIS DOSAGE AND ADMINISTRATION

Directions: At first sign of symptoms: Adults:1 tablet every 1/2 to 1 hour until symptoms lessen,then continue with standard dosage. Do not exceed 12 tablets in 24 hours.

Standard dosage: Adults: 3tablets per day, taking 1 tablet every 4 to 6 hours.

For children under 18, consult your healthcare provider.

Allow tablets to dissolve completely in the mouth, do not swallow.

ACTIVE INGREDIENT

Active Ingredients: Each tablet contains: *Arnica montana, radix 6X, *Berberis vulgaris 8X, *Bryonia alba 4X, 8X, 12X, 30X, Causticum 8X, *Colocynthis 5X, *Dulcamara 6X, Ferrum phosphoricum 12X, *Ledum palustre 6X, *Lycopodium clavatum 10X, *Ranunculus bulbosus 6X, *Rhododendron chrysanthum 8X, *Rhus toxicodendron 4X, 8X, 12X, 30X, *Sulphur 10X 15.8 mg each.

*Natural ingredients

INACTIVE INGREDIENT

Inactive Ingredients: Lactose, Magnesium stearate

BHI ARTHRITIS INDICATIONS AND USAGE

 Relieves:

  • Arthritis Pain
  • Joint Stiffness

PURPOSE

Uses: For the temporary relief of minor arthritis pain, joint stiffness.

BHI Arthritis

BHI Arthritis

ARNICA MONTANA ROOT, BERBERIS VULGARIS ROOT BARK , BRYONIA ALBA ROOT, CAUSTICUM, CITRULLUS COLOCYNTHIS FRUIT PULP, SOLANUM DULCAMARA TOP, FERROSOFERRIC PHOSPHATE, LEDUM PALUSTRE TWIG, LYCOPODIUM CLAVATUM SPORE, RANUNCULUS BULBOSUS, RHODODENDRON AUREUM LEAF,TOXICODENDRON PUBESCENS LEAF and SULFUR TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:50114-4291
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ARNICA MONTANA ROOT ARNICA MONTANA ROOT 6 [hp_X]
BERBERIS VULGARIS ROOT BARK BERBERIS VULGARIS ROOT BARK 8 [hp_X]
BRYONIA ALBA ROOT BRYONIA ALBA ROOT 4 [hp_X]
CAUSTICUM CAUSTICUM 8 [hp_X]
CITRULLUS COLOCYNTHIS FRUIT PULP CITRULLUS COLOCYNTHIS FRUIT PULP 5 [hp_X]
Solanum Dulcamara Top Solanum Dulcamara Top 6 [hp_X]
FERROSOFERRIC PHOSPHATE Ferrosoferric Phosphate 12 [hp_X]
LEDUM PALUSTRE TWIG LEDUM PALUSTRE TWIG 6 [hp_X]
Lycopodium Clavatum Spore LYCOPODIUM CLAVATUM SPORE 10 [hp_X]
Ranunculus Bulbosus Ranunculus Bulbosus 6 [hp_X]
RHODODENDRON AUREUM LEAF RHODODENDRON AUREUM LEAF 8 [hp_X]
TOXICODENDRON PUBESCENS LEAF TOXICODENDRON PUBESCENS LEAF 4 [hp_X]
SULFUR SULFUR 10 [hp_X]

Inactive Ingredients

Ingredient Name Strength
LACTOSE
MAGNESIUM STEARATE

Product Characteristics

Color Size Imprint Code Shape
white 9 mm BHI;O;M ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:50114-4291-2 100 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2000-09-30


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