warnings
WARNINGS .
Leader Childrens Multi Symptom Cold
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
- Leader Childrens Multi Symptom Cold
- Generic name
- DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL
- Manufacturer
- CARDINAL HEALTH 110, LLC. DBA LEADER
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 169ff9cf-fcf5-46a6-b460-259421f2ec07
- SPL ID
- 8e10d570-5e78-4ff3-9a30-bbdba6912b74
- Version
- 3
- Effective date
- 2024-12-16
- Source export date
- 2026-09-28
- Source partition
- 1
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:14:20
| 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 | Leader Childrens Multi Symptom Cold | openfda.brand_name | |
| generic name | DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | openfda.generic_name | |
| manufacturer name | CARDINAL HEALTH 110, LLC. DBA LEADER | openfda.manufacturer_name | |
| ndc | package | 70000-0629-1 | openfda.package_ndc |
| ndc | product | 70000-0629 | openfda.product_ndc |
| ndc11 | package | 70000062901 | derived:openfda.package_ndc |
| rxcui | 1043543 | openfda.rxcui | |
| spl id | 8e10d570-5e78-4ff3-9a30-bbdba6912b74 | id | |
| spl set id | 169ff9cf-fcf5-46a6-b460-259421f2ec07 | set_id | |
| unii | 9D2RTI9KYH | openfda.unii | |
| unii | 04JA59TNSJ | 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.