warnings
WARNINGS .
QCH Adult Tussin 541
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 541
- Generic name
- GUAIFENESIN
- Manufacturer
- Chain Drug Marketing Association Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- b487f4af-ad0c-4f18-9a6b-7fd386b3f46c
- SPL ID
- b487f4af-ad0c-4f18-9a6b-7fd386b3f46c
- Version
- 1
- Effective date
- 2024-05-02
- Source export date
- 2026-09-28
- 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/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:14:45
| 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 541 | openfda.brand_name | |
| generic name | GUAIFENESIN | openfda.generic_name | |
| manufacturer name | Chain Drug Marketing Association Inc. | openfda.manufacturer_name | |
| ndc | package | 83324-024-04 | openfda.package_ndc |
| ndc | product | 83324-024 | openfda.product_ndc |
| ndc11 | package | 83324002404 | derived:openfda.package_ndc |
| rxcui | 310604 | openfda.rxcui | |
| spl id | b487f4af-ad0c-4f18-9a6b-7fd386b3f46c | id | |
| spl set id | b487f4af-ad0c-4f18-9a6b-7fd386b3f46c | set_id | |
| 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.