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

Menu
Search

BHI Mucus

Heel Inc

BHI Mucus


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

KEEP OUT OF REACH OF CHILREN


Keep out of reach of children

BHI MUCUS INDICATIONS AND USAGE

Relieves:

• Chest Congestion

• Mucus Build-up

• Cough

WARNINGS

Warnings: If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. Ask a doctor if you have a cough that occurs with too much phlegm (mucus) or a cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis, or emphysema. Stop and ask a doctor if cough lasts for more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition. Do not use if known sensitivity to Mucus Relief or any of its ingredients exists.

DOSAGE

Directions: 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 your healthcare provider.

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

ACTIVE INGREDIENTS

Active Ingredients: Each tablet contains Antimonium tartaricum 5X, *Belladonna 6X, *Bryonia alba 6X, *Hepatica triloba 6X, *Hyoscyamus niger 5X, *Ipecacuanha 6X, *Lobelia inflata 4X, *Pertussinum 30X, *Sticta pulmonaria 5X 33.3 mg each.

*Natural ingredients

INACTIVE INGREDIENTS

Inactive Ingredients: Lactose, Magnesium stearate

PURPOSE

Uses: For the temporary relief of minor chest congestion and cough due to mucus build-up

BHI Mucus

BHI Mucus

ANTIMONY POTASSIUM TARTRATE,ATROPA BELLADONNA,BRYONIA ALBA ROOT,ANEMONE AMERICANA,HYOSCYAMUS NIGER,IPECAC,LOBELIA INFLATA,HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED, and LOBARIA PULMONARIA TABLET

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:50114-6922
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Antimony Potassium Tartrate ANTIMONY CATION (3+) 5 [hp_X]
ATROPA BELLADONNA ATROPA BELLADONNA 6 [hp_X]
BRYONIA ALBA ROOT BRYONIA ALBA ROOT 6 [hp_X]
ANEMONE AMERICANA ANEMONE AMERICANA 6 [hp_X]
Hyoscyamus Niger HYOSCYAMUS NIGER 5 [hp_X]
Ipecac IPECAC 6 [hp_X]
LOBELIA INFLATA LOBELIA INFLATA 4 [hp_X]
HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED 30 [hp_X]
LOBARIA PULMONARIA LOBARIA PULMONARIA 5 [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:50114-6922-2 100 in 1 BOTTLE

Marketing Information

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


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.