warnings
WARNINGS .
Rugby Mucus and Chest Congestion 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
- Rugby Mucus and Chest Congestion 541
- Generic name
- GUAIFENESIN
- Manufacturer
- Rugby Laboratories
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 76472912-b66f-4bb4-937a-4a589683a78c
- SPL ID
- 0c07f9eb-4c55-4786-a2d8-bfc588e6fa2f
- Version
- 2
- Effective date
- 2026-05-04
- Source export date
- 2026-09-28
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:08:31
| 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 | Rugby Mucus and Chest Congestion 541 | openfda.brand_name | |
| generic name | GUAIFENESIN | openfda.generic_name | |
| manufacturer name | Rugby Laboratories | openfda.manufacturer_name | |
| ndc | package | 0536-1430-97 | openfda.package_ndc |
| ndc | product | 0536-1430 | openfda.product_ndc |
| ndc11 | package | 00536143097 | derived:openfda.package_ndc |
| rxcui | 1606850 | openfda.rxcui | |
| spl id | 0c07f9eb-4c55-4786-a2d8-bfc588e6fa2f | id | |
| spl set id | 76472912-b66f-4bb4-937a-4a589683a78c | 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.