warnings
WARNING .
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
- MUCUS RELIEF
- Generic name
- GUAIFENESIN
- Manufacturer
- YYBA Corp
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 5074b172-311b-43e2-e063-6394a90aa70f
- SPL ID
- 54de9af1-bbc6-ee59-e063-6394a90a05b0
- Version
- 2
- Effective date
- 2026-06-22
- Source export date
- 2026-10-30
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/0b630a6825fc0c8abba22d7c8fd4d069bde78bef928766047ddbb369119f337f/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 18:59:45
| 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 applno | ANDA | 209215 | derived:openfda.application_number |
| application number | ANDA209215 | openfda.application_number | |
| brand name | MUCUS RELIEF | openfda.brand_name | |
| generic name | GUAIFENESIN | openfda.generic_name | |
| manufacturer name | YYBA Corp | openfda.manufacturer_name | |
| ndc | package | 73581-403-03 | openfda.package_ndc |
| ndc | package | 73581-403-01 | openfda.package_ndc |
| ndc | product | 73581-403 | openfda.product_ndc |
| ndc11 | package | 73581040303 | derived:openfda.package_ndc |
| ndc11 | package | 73581040301 | derived:openfda.package_ndc |
| rxcui | 310621 | openfda.rxcui | |
| spl id | 54de9af1-bbc6-ee59-e063-6394a90a05b0 | id | |
| spl set id | 5074b172-311b-43e2-e063-6394a90aa70f | 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.