warnings
Warnings
basic care tussin dm max
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
- basic care tussin dm max
- Generic name
- DEXTROMETHORPHAN HBR, GUAIFENESIN
- Manufacturer
- Amazon.com Services LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- c6863e31-e1b9-40ff-ae2e-4aec86b4acc0
- SPL ID
- 9f3e5ffc-63c2-4a6b-8b50-e8126da3d60d
- Version
- 3
- Effective date
- 2024-11-05
- Source export date
- 2026-09-28
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:24:53
| 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 | basic care tussin dm max | openfda.brand_name | |
| generic name | DEXTROMETHORPHAN HBR, GUAIFENESIN | openfda.generic_name | |
| manufacturer name | Amazon.com Services LLC | openfda.manufacturer_name | |
| ndc | package | 72288-293-34 | openfda.package_ndc |
| ndc | product | 72288-293 | openfda.product_ndc |
| ndc11 | package | 72288029334 | derived:openfda.package_ndc |
| rxcui | 1020138 | openfda.rxcui | |
| spl id | 9f3e5ffc-63c2-4a6b-8b50-e8126da3d60d | id | |
| spl set id | c6863e31-e1b9-40ff-ae2e-4aec86b4acc0 | 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.