warnings
Warnings Ask doctor before use if you have persistent or chronic cough, such as occurs with smoking, asthma, bronchitis or emphysema cough is accompanied by excessive phlegm (mucus)
Quality Choice Mucus Relief
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
- Quality Choice Mucus Relief
- Generic name
- GUAIFENESIN
- Manufacturer
- Chain Drug Marketing Association
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 41f88b43-3e0a-4650-b167-a72afe6177e8
- SPL ID
- e8f6721f-0337-445c-84b2-592329d0ba32
- Version
- 4
- Effective date
- 2024-12-18
- 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 02:41:18
| 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 | M012 | openfda.application_number | |
| brand name | Quality Choice Mucus Relief | openfda.brand_name | |
| generic name | GUAIFENESIN | openfda.generic_name | |
| manufacturer name | Chain Drug Marketing Association | openfda.manufacturer_name | |
| ndc | package | 63868-998-50 | openfda.package_ndc |
| ndc | product | 63868-998 | openfda.product_ndc |
| ndc11 | package | 63868099850 | derived:openfda.package_ndc |
| rxcui | 359601 | openfda.rxcui | |
| spl id | e8f6721f-0337-445c-84b2-592329d0ba32 | id | |
| spl set id | 41f88b43-3e0a-4650-b167-a72afe6177e8 | 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.