Drugplain

Chlo Tuss 12.5 mg/5mL

Chlophedianol Hydrochloride, Dexbrompheniramine Maleate, Pseudoephedrine Hydrochloride · LIQUID · R.A. McNeil Company

No Recall History
Plain English

Chlo Tuss is a liquid containing chlophedianol hydrochloride, dexbrompheniramine maleate, pseudoephedrine hydrochloride at 12.5 mg/5mL, taken oral. Manufactured by R.A. McNeil Company.

Key Facts

Brand Name
Chlo Tuss
Generic Name
Chlophedianol Hydrochloride, Dexbrompheniramine Maleate, Pseudoephedrine Hydrochloride
NDC Code (Product)
12830-762
Manufacturer
R.A. McNeil Company
Strength
12.5 mg/5mL
Dosage Form
LIQUID
Route
ORAL
Marketing Status
Application #
M012
Marketing Start
10/01/2013

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

anxiety2 reports
cough2 reports
diarrhoea2 reports
drug ineffective2 reports
malaise2 reports
muscle spasms2 reports
pre-existing condition improved2 reports
product dose omission issue2 reports
sinus disorder2 reports
somnolence2 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses temporarily relieves these symptoms due to the common cold, hay fever (allergic rhinitis) or other upper respiratory allergies: cough due to minor throat and bronchial irritation runny nose sneezing itching of the nose or throat itchy, watery eyes nasal congestion reduces swelling of nasal passages

Dosage & Administration

Directions Do not exceed recommended dosage. Adults and children 12 years of age and over: 2 teaspoonfuls (10 mL) every 6 hours, not to exceed 8 teaspoonfuls in 24 hours Children 6 to under 12 years of age: 1 teaspoonful (5 mL) every 6 hours, not to exceed 4 teaspoonfuls in 24 hours Children under 6 years of age: Consult a doctor

Warnings

Warnings Do not exceed recommended dosage. Do not use this product 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 your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product Ask a doctor before use if you have a cough that lasts or is chronic such as occurs with smoking, asthma or emphysema a cough that occurs with too much phlegm (mucus) a breathing problem such as emphysema or chronic bronchitis glaucoma trouble urinating due to an enlarged prostate gland heart disease high blood pressure thyroid disease diabetes Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers. When using this product excitability may occur, especially in children may cause marked drowsiness avoid alcoholic drinks alcohol, sedatives, and tranquilizers may increase the drowsiness effect be careful when driving a motor vehicle or operating machinery Stop use and ask a doctor if nervousness, dizziness, or sleeplessness occur cough or nasal congestion persists for m

Frequently Asked Questions

What is Chlo Tuss used for?

Chlo Tuss contains Chlophedianol Hydrochloride, Dexbrompheniramine Maleate, Pseudoephedrine Hydrochloride. It is a liquid taken oral. Consult your doctor for specific uses.

Is Chlo Tuss a controlled substance?

Chlo Tuss is not classified as a controlled substance by the DEA.

What is the generic name for Chlo Tuss?

The generic name for Chlo Tuss is Chlophedianol Hydrochloride, Dexbrompheniramine Maleate, Pseudoephedrine Hydrochloride. There are no other listed brand versions of Chlophedianol Hydrochloride, Dexbrompheniramine Maleate, Pseudoephedrine Hydrochloride.

What is the NDC code for Chlo Tuss 12.5 mg/5mL?

The NDC (National Drug Code) for Chlo Tuss 12.5 mg/5mL is 12830-762, listed by R.A. McNeil Company.

Product NDC

12830-762

Package NDC

12830-762-15

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)