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

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Broncotron

Seyer Pharmatec, Inc.
Seyer Pharmatec, Inc.

Drug Facts




FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredients(in each 5 mL teaspoonful) .......................................... Purpose

Dextromethorphan HBR, 10 mg..................................................................Cough suppressant

Purpose

Uses:

  • temporarily relieves cough due to minor throat and bronchial irritations as may occur with a cold.
  • helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive.

Warnings:

Ask a 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, bronchitis, or emphysema.
Stop use and ask a doctor if:

  • Cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache. A persistent cough may be a sign of a serious condition.

Do not use if you are now taking a prescription monoamine oxidase (MOAI) (certain drugs for depression, pychiatric, or emotional conditions, or Parkison's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

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

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

Directions

  • do not take more than 6 doses in any 24-hour period, unless directed by a physician.

Age Doses
 adults and children 12 years and over
 2 teaspoonfuls every 4 hours
 children 6 years to under 12 years
 1 teaspoonful every 4 hours
 children under 6 years
 ask a doctor

Uses

Other information:

  • Phenylketonuric: contains Phenylalanine 35mg/5mL
  • store at room temperature.


Inactive ingrdients:

Questions or Comments call: 1(800) 782- 3585.

Broncotron

Broncotron

Dextromethorphan, Guaifenesin LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:11026-2640
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DEXTROMETHORPHAN HYDROBROMIDE DEXTROMETHORPHAN 10 mg
Guaifenesin GUAIFENESIN 100 mg

Inactive Ingredients

Ingredient Name Strength
ASPARTAME
CITRIC ACID MONOHYDRATE
POLYGLYCERIN-10
HYDROXYETHYL CELLULOSE (2000 CPS AT 1%)
METHYLPARABEN
SODIUM CITRATE
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:11026-2640-4 118 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 1998-01-01


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