warnings
Warnings
tussin
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
- tussin
- Generic name
- DEXTROMETHORPHAN HBR, GUAIFENESIN
- Manufacturer
- H E B
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 7c24c59c-7549-4c64-95f8-4bf755cd6f61
- SPL ID
- 5ad97f47-bc42-4590-9c7a-f0cd28a24cc1
- Version
- 3
- Effective date
- 2024-11-05
- Source export date
- 2026-10-12
- 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/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:31:06
| 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 | tussin | openfda.brand_name | |
| generic name | DEXTROMETHORPHAN HBR, GUAIFENESIN | openfda.generic_name | |
| manufacturer name | H E B | openfda.manufacturer_name | |
| ndc | package | 37808-639-34 | openfda.package_ndc |
| ndc | package | 37808-639-26 | openfda.package_ndc |
| ndc | product | 37808-639 | openfda.product_ndc |
| ndc11 | package | 37808063934 | derived:openfda.package_ndc |
| ndc11 | package | 37808063926 | derived:openfda.package_ndc |
| rxcui | 1020138 | openfda.rxcui | |
| spl id | 5ad97f47-bc42-4590-9c7a-f0cd28a24cc1 | id | |
| spl set id | 7c24c59c-7549-4c64-95f8-4bf755cd6f61 | set_id | |
| unii | 9D2RTI9KYH | openfda.unii | |
| 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.