Tukol A
Tukol A is an FDA drug label for the active ingredient DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE manufactured by Genomma Lab USA, Inc. administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20171228.
Generic: DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE
Manufacturer: Genomma Lab USA, Inc.
Product Type: HUMAN OTC DRUG
Route: ORAL
Dosage Form:
NDC: 50066-536
Application: part341
Effective: 20171228
Active Ingredients: Active ingredients DRUG FACTS Active ingredients (in each 5 mL, 1 teaspoon) Dextromethorphan HBr, USP 5 mg Guaifenesin, USP 50 mg Phenylephrine HCL, USP 2.5 mg
Indications & Usage
Uses help loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes temporarily relieves these symptoms occurring with a cold - nasal congestion - cough due to minor throat and bronchial irritation
Dosage & Administration
Directions age dose children 6 to 12 years 2 tsp (10 mL) every 4 hours children 4 to 6 years 1 tsp (5 mL) every 4 hours children under 4 years do not use do not exceed 6 doses in a 24-hour period use enclosed dosage cup tsp = teaspoon, mL = milliliter
Contraindications
Not available.
Warnings
Warnings Do not use in a child who is 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 your child's prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.
Adverse Reactions
Not available.
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