warnings
Warnings
Tussin DM
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 DM
- Generic name
- DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE
- Manufacturer
- CVS Pharmacy
- Product type
- HUMAN OTC DRUG
- SPL set ID
- fc1e224c-5c57-43fc-ae6e-36aa0a4ae439
- SPL ID
- faf0eaea-ff1c-411f-b7ad-f0362d7d9b32
- Version
- 5
- Effective date
- 2025-08-06
- Source export date
- 2026-10-12
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:38:10
| 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 DM | openfda.brand_name | |
| generic name | DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE | openfda.generic_name | |
| manufacturer name | CVS Pharmacy | openfda.manufacturer_name | |
| ndc | package | 69842-699-26 | openfda.package_ndc |
| ndc | product | 69842-699 | openfda.product_ndc |
| ndc11 | package | 69842069926 | derived:openfda.package_ndc |
| rxcui | 1115329 | openfda.rxcui | |
| spl id | faf0eaea-ff1c-411f-b7ad-f0362d7d9b32 | id | |
| spl set id | fc1e224c-5c57-43fc-ae6e-36aa0a4ae439 | set_id | |
| unii | 9D2RTI9KYH | openfda.unii | |
| unii | V9BI9B5YI2 | 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.