Codeine / Guaifenesin / Pseudoephedrine Dosage
Medically reviewed by Drugs.com. Last updated on Jan 6, 2020.
Applies to the following strengths: 10 mg-100 mg-30 mg/5 mL; 20 mg-200 mg-60 mg/5 mL; 10 mg-100 mg-22.5 mg/5 mL; 9 mg-200 mg-30 mg/5 mL; 10 mg-400 mg-60 mg; 20 mg-400 mg-60 mg; 10 mg-400 mg-40 mg; 20 mg-400 mg-40 mg; 10 mg-400 mg-20 mg; 20 mg-400 mg-20 mg; 10 mg-400 mg-30 mg; 20 mg-400 mg-30 mg; 8 mg-200 mg-30 mg/5 mL
Usual Adult Dose for:
Additional dosage information:
Usual Adult Dose for Cold Symptoms
1 dose orally every 4 to 6 hours as needed
-Codeine: Single dose: up to 20 mg; Maximum daily dose: 120 mg in 24 hours
-Guaifenesin: Single dose: up to 400 mg; Maximum daily dose: 2400 mg in 24 hours
-Pseudoephedrine: Single dose: up to 60 mg; Maximum daily dose: 240 mg in 24 hours
-Maximum dose should not exceed maximum dose of any of the single ingredient doses.
-Oral liquid should be measured with an accurate milliliter measuring device.
Uses: Temporary relief of coughs due to the common cold, allergic rhinitis or other upper respiratory allergies; reduces swelling of nasal passages to relieve nasal congestion and helps loosen mucus and thin bronchial secretions to make cough more productive.
Renal Dose Adjustments
Dose adjustments not recommended
Liver Dose Adjustments
Dose adjustments not recommended
The US FDA requires a Risk Evaluation and Mitigation Strategy (REMS) for all opioids intended for outpatient use. The new FDA Opioid Analgesic REMS is a designed to assist in communicating the serious risks of opioid pain medications to patients and health care professionals. It includes a medication guide and elements to assure safe use. For additional information: www.accessdata.fda.gov/scripts/cder/rems/index.cfm
-Opioid Analgesic REMS: To ensure that the benefits of opioid analgesics outweigh the risks of addiction, abuse, and misuse, a REMS is required for these products. Under the requirements of the REMS, drug companies with approved opioid analgesic products must make REMS-compliant education programs available to healthcare providers. Healthcare providers are strongly encouraged to complete a REMS-compliant education program; counsel patients and/or their caregivers, with every prescription on safe use, serious risks, storage, and disposal of these products; emphasize to patients and their caregivers the importance of reading the Medication Guide every time it is provided by their pharmacist, and consider other tools to improve patient, household, and community safety.
The US FDA recommends against use of codeine-containing cough and cold medications in patients less than 18 years because it has been determined that the risks outweigh benefits.
Consult WARNINGS section for additional precautions.
US Controlled Substance: Schedule V
Data not available
-Take orally with or without food
-Oral measuring devices should be provided to ensure accuracy in dosing; a household teaspoon should not be considered an accurate measuring device
-Protect from moisture and light
-Patients who are ultra-rapid metabolizers of codeine due to a CYP450 2D6 polymorphism, will convert codeine more rapidly and completely to morphine resulting in unexpectedly high morphine levels, which may be life-threatening.
-Codeine use is contraindicated in the postoperative period in children who have undergone tonsillectomy and/or adenoidectomy.
-Cardiovascular: Monitor for signs of hypotension, especially in those whose blood pressure is compromised
-Respiratory: Monitor for respiratory depression
-Gastrointestinal: Monitor for constipation and decreased bowel motility in post-operative patients.
-Patients should be monitored for the development of addiction, abuse, or misuse.
-Patients should understand that codeine use can result in addiction, abuse, and misuse; recommended doses should not be exceeded.
-Patients should be understand that this product is for temporary relief of cough; if cough persists for longer than 1 week, recurs, or is accompanied by fever, rash, or persistent headache, a health care professional should be consulted.
-Patients should understand risks of life-threatening respiratory depression and when this risk is greatest; patients should be aware that a genetic mutation may result in greater codeine toxicity in some patients; breastfed infants of women who have this genetic mutation are also at risk.
-Women who are breastfeeding, pregnant, or planning to become pregnant should speak to their healthcare provider before using this product.
-This drug may cause drowsiness, dizziness, or impair thinking or motor skills; patients should avoid driving or operating machinery until adverse effects are determined.
-Concomitant use of alcohol, sedatives, and tranquilizers may increase drowsiness; patients should avoid alcohol and consult with their healthcare provider regarding concomitant use of other CNS depressants.
-Patients should be instructed to discontinue use if they experience nervousness, dizziness, or sleeplessness.
-Patients should be instructed to read the US FDA-approved Medication Guide each time this drug is dispensed; they should understand the safe use, serious risks, and proper storage and disposal of this drug.
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
More about codeine / guaifenesin / pseudoephedrine
- Side Effects
- During Pregnancy
- Drug Interactions
- En Español
- 1 Review
- Drug class: upper respiratory combinations
- FDA Alerts (6)