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

Bronchial Cough

Apotheca Company

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert
Bronchial Cough



FULL PRESCRIBING INFORMATION

Active ingredient

ACTIVE INGREDIENTS:  Coccus cacti 4X, Drosera 4X, Scilla maritima 4X, Arsenicum iodatum 6X, Causticum 6X, Carbo vegetabilis 12X, Kali carbonicum 12X, Lachesis mutus 12.


Purpose

INDICATIONS:  For temporary relief of symptoms related to bronchial cough including irritating cough, difficult breathing, congestion, and respiratory inflammation.


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

INDICATIONS:  For temporary relief of symptoms related to bronchial cough including irritating cough, difficult breathing, congestion, and respiratory inflammation.


Dist. By:

Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84070

www.desbio.com


DESBIO

NDC 57520-0932-1

HOMEOPATHIC

BRONCHIAL COUGH

1 FL OZ (30 ml)

Bronchial Cough

Coccus cacti, Drosera, Scilla maritima, Arsenicum iodatum, Causticum, Cuprum aceticum, Carbo vegetabilis, Kali Carbonicum, Lachesis mutus, LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:57520-0932
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
PROTORTONIA CACTI PROTORTONIA CACTI 4 [hp_X]
DROSERA ROTUNDIFOLIA DROSERA ROTUNDIFOLIA 4 [hp_X]
Drimia Maritima Bulb DRIMIA MARITIMA BULB 4 [hp_X]
ARSENIC TRIIODIDE ARSENIC TRIIODIDE 6 [hp_X]
CAUSTICUM CAUSTICUM 6 [hp_X]
CUPRIC ACETATE CUPRIC CATION 6 [hp_X]
Activated Charcoal ACTIVATED CHARCOAL 12 [hp_X]
POTASSIUM CARBONATE CARBONATE ION 12 [hp_X]
LACHESIS MUTA VENOM LACHESIS MUTA VENOM 12 [hp_X]

Inactive Ingredients

Ingredient Name Strength
water
ALCOHOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:57520-0932-1 30 in 1 BOTTLE, DROPPER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2011-10-28


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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