warnings
WARNING .
Childrens 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
- Childrens Cough
- Generic name
- DEXTROMETHORPHAN HBR, GUAIFENESIN
- Manufacturer
- Wal-Mart Stores, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 50a0eaa5-fa73-4d84-86fc-3546c85cf353
- SPL ID
- 9cbd6363-5acb-4d86-ad1f-d99dca1655d2
- Version
- 4
- Effective date
- 2024-12-20
- Source export date
- 2026-10-30
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/9abf0f8b126f8aad070e21ea702bfb5e39ce670b16ae57dd52e8877705d1bf5d/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:26:57
| 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 | Childrens Cough | openfda.brand_name | |
| generic name | DEXTROMETHORPHAN HBR, GUAIFENESIN | openfda.generic_name | |
| manufacturer name | Wal-Mart Stores, Inc. | openfda.manufacturer_name | |
| ndc | package | 49035-773-03 | openfda.package_ndc |
| ndc | product | 49035-773 | openfda.product_ndc |
| ndc11 | package | 49035077303 | derived:openfda.package_ndc |
| rxcui | 1020138 | openfda.rxcui | |
| spl id | 9cbd6363-5acb-4d86-ad1f-d99dca1655d2 | id | |
| spl set id | 50a0eaa5-fa73-4d84-86fc-3546c85cf353 | 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.