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

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Broncomar

Gadal Laboratories Inc




FULL PRESCRIBING INFORMATION

Active ingredient

Acvtive ingredients: (in 10 ml)              Purpose

Acetaminophen 200 mg ............................. Analgesic

Dextromethorphan HBr 13.33 mg ................... Cough Suppressant

Guaifenesin 200 mg ................................... Expectorant

Phenylephrine HCl 5 mg ............................. Decongestant

Purpose

Purpose

Analgesic

Cough Suppressant

Expectorant

Decongestant

Uses

Uses

  • For temporary relief of bronchial and nasal congestion
  • Help loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes and make cough more productive.
  • Teporarily relieves cough due to minor throat and bronchial irritation as may occur with the common cold

Warnings

Do not exceed recommended dosage

Liver warning: This product contains Acetaminophen. Sever liver damage may occur if

  • Adult takes more than 6 doses in 24 hours, which is the maximum daily amount
  • Child takes more than 5 doses in 24 hours
  • Taken with other drugs containing Acetaminophen
  • Adult has 3 or more alcoholic drinks everyday while using this product
  • Do not give to children under 3 years of age or use for more than 10 days unless directed by a physician

Do not use

  • If you are now taking a prescription monoamine oxidase inhibitor (MAOI)( certain drugs for depression , psychiatric conditions, or Parkinson’s disease) or for 2 weeks after stopping the MAOI drug.
  • if you do not know if your prescription drug contains on MAOI ask your doctor or pharmacist before taking this product
  • if you have a chronic pulmonary disease or shortness of breath unless directed by a doctor
  • avoid alcoholic beverages while you are taking this product
  • do not use with any other drug containing Acetaminophen (prescirption or nonprescription). If you are not sure whether a drug contains Acetaminophen, ask a doctor or a pharmacist.

Ask the doctor before use if you have

  • cough that occurs with too much phlegm (mucus)
  • cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis or emphysema
  • heart disease, high blood pressure, thyroid disease, or difficulty in urination due to the enlargement of prostate gland.
  • The user has liver disease
  • The user is taking the blood thinning drug Warfarin.

Stop use and ask the doctor if

  • Nervoisness, dizziness or sleeplessness occurs.
  • Cough persists for more than 1 week, tends to recur, or accompanied by fever, rash or persistent headache. A persistent cough may be sign of a serious condition

If pregnant or breast-feeding, ask a health professional before use. 

 

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

  • Do not take more than 6 doses in any 24-hour period

Age                                                                        Dose

Adults and children 12 years and over           10 mL (2 tsps) every 6 hours

Children 6 to under 12 years of age.               5 mL (1 tsps) every 6 hours

Children under 6 years of age                       Do not use

Inactive ingredients

Aloe vera, citric acid, disodium EDTA, FD&C Red #40, hydroxyethyl cellulose, natural strawberry flavor, propylene glycol, water, sodium benzoate, sorbitol 70%, sucralose

Broncomar

Broncomar

Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:53113-215
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ACETAMINOPHEN ACETAMINOPHEN 250 mg
DEXTROMETHORPHAN HYDROBROMIDE DEXTROMETHORPHAN 13.33 mg
Guaifenesin GUAIFENESIN 200 mg
Phenylephrine Hydrochloride PHENYLEPHRINE 5 mg

Inactive Ingredients

Ingredient Name Strength
ALOE VERA WHOLE
ANHYDROUS CITRIC ACID
EDETATE DISODIUM
FD&C RED NO. 40
HYDROXYMETHYL CELLULOSE
water
SODIUM BENZOATE
sorbitol
Sucralose
propylene glycol

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 177 in 1 BOTTLE
2 NDC:53113-215-06 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2014-06-01


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Be sure to consult your doctor before taking any medication!
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