warnings
WARNINGS .
QCH Adult Tussin DM 542
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
- Brand name
- QCH Adult Tussin DM 542
- Generic name
- DEXTROMETHORPHAN HBR, GUAIFENESIN
- Manufacturer
- Chain Drug Marketing Association Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 17caffa4-a264-7f3e-e063-6394a90ac419
- SPL ID
- 41a95b6d-6e0a-4729-ac06-3963a78a0e51
- Version
- 2
- Effective date
- 2024-05-08
- Source export date
- 2026-10-12
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:39:17
| Harmonized routes |
|---|
| ORAL |
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 |
|---|---|---|---|
| application number | part341 | openfda.application_number | |
| brand name | QCH Adult Tussin DM 542 | openfda.brand_name | |
| generic name | DEXTROMETHORPHAN HBR, GUAIFENESIN | openfda.generic_name | |
| manufacturer name | Chain Drug Marketing Association Inc. | openfda.manufacturer_name | |
| ndc | package | 83324-023-08 | openfda.package_ndc |
| ndc | package | 83324-023-04 | openfda.package_ndc |
| ndc | product | 83324-023 | openfda.product_ndc |
| ndc11 | package | 83324002308 | derived:openfda.package_ndc |
| ndc11 | package | 83324002304 | derived:openfda.package_ndc |
| rxcui | 1790650 | openfda.rxcui | |
| spl id | 41a95b6d-6e0a-4729-ac06-3963a78a0e51 | id | |
| spl set id | 17caffa4-a264-7f3e-e063-6394a90ac419 | set_id | |
| unii | 9D2RTI9KYH | openfda.unii | |
| unii | 495W7451VQ | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.