warnings
WARNINGS SECTION
Guaifenesin 1200 mg
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
- Guaifenesin 1200 mg
- Generic name
- GUAIFENESIN 1200 MG
- Manufacturer
- MARKSANS PHARMA LIMITED
- Product type
- HUMAN OTC DRUG
- SPL set ID
- fedf43d0-d6d1-4f50-bbab-396701e45cb2
- SPL ID
- 0af3bdb4-c1f3-4941-a1de-6e08c49849cb
- Version
- 6
- Effective date
- 2025-10-17
- Source export date
- 2026-10-12
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:13:01
| 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 | 217780 | derived:openfda.application_number |
| application number | ANDA217780 | openfda.application_number | |
| brand name | Guaifenesin 1200 mg | openfda.brand_name | |
| brand name | Guaifenesin 600 mg | openfda.brand_name | |
| generic name | GUAIFENESIN 1200 MG | openfda.generic_name | |
| generic name | GUAIFENESIN 600 MG | openfda.generic_name | |
| manufacturer name | MARKSANS PHARMA LIMITED | openfda.manufacturer_name | |
| ndc | package | 25000-041-75 | openfda.package_ndc |
| ndc | package | 25000-041-34 | openfda.package_ndc |
| ndc | package | 25000-041-12 | openfda.package_ndc |
| ndc | package | 25000-042-55 | openfda.package_ndc |
| ndc | package | 25000-042-99 | openfda.package_ndc |
| ndc | package | 25000-042-12 | openfda.package_ndc |
| ndc | package | 25000-042-01 | openfda.package_ndc |
| ndc | product | 25000-042 | openfda.product_ndc |
| ndc | product | 25000-041 | openfda.product_ndc |
| ndc11 | package | 25000004112 | derived:openfda.package_ndc |
| ndc11 | package | 25000004134 | derived:openfda.package_ndc |
| ndc11 | package | 25000004212 | derived:openfda.package_ndc |
| ndc11 | package | 25000004299 | derived:openfda.package_ndc |
| ndc11 | package | 25000004175 | derived:openfda.package_ndc |
| ndc11 | package | 25000004255 | derived:openfda.package_ndc |
| ndc11 | package | 25000004201 | derived:openfda.package_ndc |
| rxcui | 636522 | openfda.rxcui | |
| rxcui | 310621 | openfda.rxcui | |
| spl id | 0af3bdb4-c1f3-4941-a1de-6e08c49849cb | id | |
| spl set id | fedf43d0-d6d1-4f50-bbab-396701e45cb2 | 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.