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

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BHI Allergy

Heel Inc

BHI Allergy Tablet


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

KEEP OUT OF REACH OF CHILDREN


Keep out of reach of children

INDICATION AND USAGE

For the temporary relief of minor allergy symptoms:

  •  Runny Nose
  • Watery Eyes due to Hayfever
  • Mild Skin Rashes and Hives

WARNINGS

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

BHI ALLERGY DOSAGE AND ADMINISTRATION

At first sign of symptoms: Adults and children 4 years and older: 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 and children 4 years and older: 3 tablets per day, taking 1 tablet every 4 to 6 hours. For children under 4, consult you healthcare provider.

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

ACTIVE INGREDIENTS

Active Ingredients:

Each tablet contains: Antimonium crudum 10X, *Arnica montana, radix 6X, Formicumacidum 8X, Graphites 10X, Histaminum hydrochloricum 8X, 12X, 30X, 200X, *Ignatia amara 6X, *Lappa major 8X, *Ledum palustre 8X, *Lycopodium clavatum 6X, *Pix liquida 10X, Selenium metallicum 12X, *Sulphur 12X, Sulphuricum acidum 30X, *Tellurium metallicum 10X, *Thuja occidentalis 6X 16.7 mg each.

*Natural ingredients

INACTIVE INGREDIENTS

Inactive Ingredients: Lactose, Magnesium stearate

PURPOSE

Relieves:

• Runny Nose

• Watery Eyes due to Hayfever

• Mild Skin Rashes & Hives

BHI Allergy

BHI Allergy

ANTIMONY TRISULFIDE, ARNICA MONTANA ROOT, FORMIC ACID, GRAPHITE, HISTAMINE DIHYDROCHLORIDE,STRYCHNOS IGNATII SEED, ARCTIUM LAPPA ROOT, LEDUM PALUSTRE TWIG, LYCOPODIUM CLAVATUM SPORE, PINE TAR, SELENIUM, SULFUR, SULFURIC ACID, TELLURIUM, THUJA OCCIDENTALIS LEAFY TWIG TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:50114-4286
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Antimony Trisulfide Antimony Trisulfide 10 [hp_X]
ARNICA MONTANA ROOT ARNICA MONTANA ROOT 6 [hp_X]
Formic Acid 8 [hp_X]
Graphite GRAPHITE 10 [hp_X]
HISTAMINE DIHYDROCHLORIDE Histamine 8 [hp_X]
STRYCHNOS IGNATII SEED STRYCHNOS IGNATII SEED 6 [hp_X]
ARCTIUM LAPPA ROOT ARCTIUM LAPPA ROOT 8 [hp_X]
LEDUM PALUSTRE TWIG LEDUM PALUSTRE TWIG 8 [hp_X]
Lycopodium Clavatum Spore LYCOPODIUM CLAVATUM SPORE 6 [hp_X]
Pine Tar PINE TAR 10 [hp_X]
Selenium SELENIUM 12 [hp_X]
SULFUR SULFUR 12 [hp_X]
SULFURIC ACID SULFURIC ACID 30 [hp_X]
Tellurium Tellurium 19 [hp_X]
THUJA OCCIDENTALIS LEAFY TWIG THUJA OCCIDENTALIS LEAFY TWIG 6 [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:50114-4286-2 100 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
1993-01-31


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Be sure to consult your doctor before taking any medication!
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