FDA label dbae2b29-1757-456b-8f4f-c00eda02bf07
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- SPL set ID
- 60af3ee8-75cf-4e7e-b90f-c426d6f2cabd
- SPL ID
- dbae2b29-1757-456b-8f4f-c00eda02bf07
- Version
- 1
- Effective date
- 2010-11-02
- Source export date
- 2026-09-28
- Source partition
- 9
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:01:49
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| spl id | dbae2b29-1757-456b-8f4f-c00eda02bf07 | id | |
| spl set id | 60af3ee8-75cf-4e7e-b90f-c426d6f2cabd | set_id |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
WARNINGS Do not exceed recommended dosage. If nervousness, dizziness, or sleeplessness occurs, discontinue use and consult a doctor. If symptoms do not improve within 7 days or are accompanied by a fever, consult a doctor. Tripohist™ D Liquid should be used with considerable caution in patients with glaucoma; stenosing peptic ulcer; pyloroduodenal obstruction; prostatic hypertrophy; bladder neck obstruction; hypertension; diabetes mellitus; ischemic heart disease and hyperthyroidism. Sympathomimetics may produce CNS stimulation and convulsions or cardiovascular collapse with accompanying hypotension. Do not take this product, unless directed by a physician, if you have a breathing problem such as emphysema or chronic bronchitis, or if you have glaucoma or difficulty in urination due to enlargement of the prostate gland. May cause drowsiness; alcohol, sedatives, and tranquilizers may increase the drowsiness effect. Avoid alcoholic beverages while taking this product. Do not take this product if you are taking sedatives or tranquilizers, without first consulting your physician. Use caution when driving a motor vehicle or operating machinery. Pseudoephedrine is banned and tested for by the U.S. Olympic Committee. Pediatric Use See PRECAUTIONS, Pediatric Use This product may cause excitability especially in children. Do not give this product to children who have a breathing problem such as chronic bronchitis, or who have glaucoma, without first consulting the child's physician. This product may cause drowsiness. Sedatives and tranquilizers may increase the drowsiness effect. Do not give this product to children who are taking sedatives or tranquilizers, without first consulting the child's physician.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTIONS The most frequent adverse reactions to antihistamines are sedation, dizziness, disturbed coordination, epigastric distress, and thickening of bronchial secretions. Others include vomiting, dry mouth, nervousness, nausea, anorexia, diplopia, polyuria, and diarrhea. Sympathomimetic amines may cause convulsions, CNS stimulation, cardiac arrhythmias, respiratory difficulty, tachycardia, palpitations, increased blood pressure, hallucinations, tremors, nervousness, insomnia, weakness, pallor, and dysuria.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.