warnings
Warnings
cold and cough
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
- cold and cough
- Generic name
- BROMPHENIRAMINE MALEATE, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL
- Manufacturer
- H E B
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 404ef5f4-7b7b-4c08-b159-9175a91be132
- SPL ID
- 61dc74c6-b13b-4251-a253-3affa4cbb986
- Version
- 4
- Effective date
- 2024-11-17
- Source export date
- 2026-10-12
- 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/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:52:41
| 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 | cold and cough | openfda.brand_name | |
| generic name | BROMPHENIRAMINE MALEATE, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | openfda.generic_name | |
| manufacturer name | H E B | openfda.manufacturer_name | |
| ndc | package | 37808-987-26 | openfda.package_ndc |
| ndc | product | 37808-987 | openfda.product_ndc |
| ndc11 | package | 37808098726 | derived:openfda.package_ndc |
| rxcui | 1090463 | openfda.rxcui | |
| spl id | 61dc74c6-b13b-4251-a253-3affa4cbb986 | id | |
| spl set id | 404ef5f4-7b7b-4c08-b159-9175a91be132 | set_id | |
| unii | 9D2RTI9KYH | openfda.unii | |
| unii | 04JA59TNSJ | openfda.unii | |
| unii | IXA7C9ZN03 | 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.