Biocotron –

Biocotron –

Biocotron – Recall

Get an alert when a recall is issued.

Questions & Answers

Side Effects & Adverse Reactions

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, chronic bronchitis, or emphysema.

When using this product, do not exceed recommended dosage

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 inhibitor (MAOI)
(certain drugs for depression, psychiatric or emotional conditions or
Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you
do not know if you are taking a prescription drug that contains an MAOI;
ask your doctor or pharmacist before taking this product.

Legal Issues

There is currently no legal information available for this drug.

FDA Safety Alerts

There are currently no FDA safety alerts available for this drug.

Manufacturer Warnings

There is currently no manufacturer warning information available for this drug.

FDA Labeling Changes

There are currently no FDA labeling changes available for this drug.


Other information store at controlled room temperature
20-25 C (68-77 F); excursion permitted to 15-30 C (59-86 F). Tamper
evident by imprinted heat seal under cap. Do not use if there is
evidence of tampering.
Warning: Phenylketonuric: Contains 11.25 mg of phenylalanine per 5 ml (one teaspoonful) dose.


There is currently no drug history available for this drug.

Other Information

There are no additional details available for this product.

Biocotron – Manufacturers

  • Advanced Generic Corporation
    Biocotron – (Dextromethorphan, Guaifenesin) Liquid [Advanced Generic Corporation]

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