FDA records indicate that there are no current recalls for this drug.
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Pseudoephedrine Plus Recall
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Questions & Answers
Side Effects & Adverse Reactions
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 are uncertain whether your prescription drug contains an MAOI
- a breathing problem such as emphysema or chronic bronchitis
- heart disease
- high blood pressure
- thyroid disease
- diabetes
- glaucoma
- difficulty in urination due to enlargement of the prostate gland
Stop use and ask a doctor if
- nervousness, dizziness, or sleeplessness occurs
- symptoms do not improve within 7 days or occur with a fever
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.
Uses
- temporarily relieves these symptoms due to hay fever and the common cold
- itching of the nose and throat,
- sneezing
- runny nose
- itchy, watery eyes
- nasal congestion
History
There is currently no drug history available for this drug.
Other Information
There are no additional details available for this product.
Sources
Pseudoephedrine Plus Manufacturers
-
Contract Pharmacal Corp
Pseudoephedrine Plus | Contract Pharmacal Corp
Directions
adults and children 12 years of age and over take 1 tablet every 4 to 6 hours, not to exceed 4 doses in 24 hours children 6 to 12 years of age take ½ tablet every 4 to 6 hours, not to exceed 4 doses in 24 hours children under 6 years of age consult a physicianDO NOT EXCEED RECOMMENDED DOSE
Other information
store at room temperature (59˚ – 86˚F)
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