Lungs and Bronchial Relief description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

Lungs and Bronchial Relief

King Bio Inc.
King Bio Inc.

Lungs and Bronchial Relief™




FULL PRESCRIBING INFORMATION

Active ingredient

Drug Facts​__________________________________________________________________________________________________________

HPUS active ingredients: Ammonium carbonicum, Antimonium arsenicicum, Antimonium tartaricum, Arsenicum album, Bromium, Carbo vegetabilis, Chlorinum, Kali carbonicum, Lobelia inflata, Stannum metallicum, Sulphuricum acidum. Equal volumes of each ingredient in 10X, 30X, 100X, 1M, LM1, LM2, LM3 potencies.

Uses

Uses for temporary relief of difficult breathing: lung and bronchial congestion, wheezing, hoarseness, coughing attacks, burning in chest, bronchial mucus, mucous congestion, and dry cough

Inactive Ingredients:

Bio-Energetically Enhanced™ pure water, citric acid and potassium sorbate.

Warnings

  • Stop use and ask your doctor if symptoms persist or worsen.
  • If pregnant or breast-feeding, take only on advice of a healthcare professional.
  • Keep out of reach of children.

Directions

  • Initially, depress pump until primed.
  • Spray one dose directly into mouth.
  • Adults 12 and up: 3 sprays 3 times per day.
  • Children 2-12: 2 sprays 3 times per day.
  • Children 2 mo.2 yr 1 spray 3 times per day.

Tamper resistant for your protection . Use only if seal is intact.

Purpose

Uses for temporary relief of difficult breathing:

  • lung and bronchial congestion
  • wheezing
  • hoarseness
  • couthing attacks
  • burning in chest
  • bronchial mucus
  • mucous congestion
  • dry cough

Lungs and Bronchial Relief

Lungs and Bronchial Relief

Ammonium carbonicum, Antimonium arsenicicum, Antimonium tartaricum, Arsenicum album, Bromium, Carbo vegetabilis, Chlorinum, Kali carbonicum, Lobelia inflata, Stannum metallicum, Sulphuricum acidum LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:57955-0053
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
AMMONIUM CARBONATE AMMONIA 10 [hp_X]
ANTIMONY ARSENATE ARSENATE ION 10 [hp_X]
Antimony Potassium Tartrate ANTIMONY CATION (3+) 10 [hp_X]
ARSENIC TRIOXIDE ARSENIC TRIOXIDE 10 [hp_X]
BROMINE BROMINE 10 [hp_X]
Activated Charcoal ACTIVATED CHARCOAL 10 [hp_X]
CHLORINE CHLORINE 10 [hp_X]
POTASSIUM CARBONATE CARBONATE ION 10 [hp_X]
LOBELIA INFLATA LOBELIA INFLATA 10 [hp_X]
tin Tin 10 [hp_X]
SULFURIC ACID SULFURIC ACID 10 [hp_X]

Inactive Ingredients

Ingredient Name Strength
CITRIC ACID MONOHYDRATE
POTASSIUM SORBATE
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:57955-0053-2 59 in 1 BOTTLE, SPRAY

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2014-05-05


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.