FDA records indicate that there are no current recalls for this drug.
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Nasohist Pediatric Recall
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Questions & Answers
Side Effects & Adverse Reactions
Do not exceed recommended dosage.
- 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 giving this product
- a breathing problem such as chronic bronchitis
- glaucoma
- heart disease
- high blood pressure
- thyroid disease
- diabetes mellitus
- nervousness, dizziness, or sleeplessness occur
- symptoms do not improve within 7 days or are accompanied by a fever
- new symptoms occur
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 the common cold, hay fever (allergic rhinitis) or other upper respiratory allergies:
- runny nose
- sneezing
- itching of the nose or throat
- itchy, watery eyes
- nasal congestion
- reduces swelling of nasal passages
History
There is currently no drug history available for this drug.
Other Information
There are no additional details available for this product.
Sources
Nasohist Pediatric Manufacturers
-
Hawthorn Pharmaceuticals, Inc.
Nasohist Pediatric | Hawthorn Pharmaceuticals, Inc.
Administer each dose four times per day using provided dropper.
Do not exceed recommended dosage. AGE
DOSE*
Children 6 to under
12 years of age:
2 dropperfuls (2 mL) every 4-6 hours, not to
exceed 4 doses (8 dropperfuls) per 24 hours,
or as directed by a doctor.
Children under 6
years of age:
Consult a physician.
*In mild cases or in particularly sensitive patients, less frequent or reduced doses may be adequate.
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