warnings
Warnings
Vicks DayQuil Kids and Vicks NyQuil Kids FREE OF ARTIFICIAL DYES and SUGAR COLD and COUGH plus
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
- Vicks DayQuil Kids and Vicks NyQuil Kids FREE OF ARTIFICIAL DYES and SUGAR COLD and COUGH plus
- Generic name
- DEXTROMETHORPHAN HBR, GUAIFENESIN, DIPHENHYDRAMINE HCL
- Manufacturer
- The Procter & Gamble Manufacturing Company
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 1a143600-24b0-75dc-e063-6394a90afb53
- SPL ID
- 44e9824d-1cb4-c6e9-e063-6394a90a78de
- Version
- 3
- Effective date
- 2025-12-01
- Source export date
- 2026-09-28
- 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/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:16:52
| 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 | Vicks DayQuil Kids and Vicks NyQuil Kids FREE OF ARTIFICIAL DYES and SUGAR COLD and COUGH plus | openfda.brand_name | |
| generic name | DEXTROMETHORPHAN HBR, GUAIFENESIN, DIPHENHYDRAMINE HCL | openfda.generic_name | |
| manufacturer name | The Procter & Gamble Manufacturing Company | openfda.manufacturer_name | |
| ndc | package | 84126-312-12 | openfda.package_ndc |
| ndc | package | 84126-311-06 | openfda.package_ndc |
| ndc | package | 84126-310-06 | openfda.package_ndc |
| ndc | product | 84126-312 | openfda.product_ndc |
| ndc11 | package | 84126031212 | derived:openfda.package_ndc |
| ndc11 | package | 84126031106 | derived:openfda.package_ndc |
| ndc11 | package | 84126031006 | derived:openfda.package_ndc |
| rxcui | 2685488 | openfda.rxcui | |
| rxcui | 1014005 | openfda.rxcui | |
| rxcui | 2685490 | openfda.rxcui | |
| spl id | 44e9824d-1cb4-c6e9-e063-6394a90a78de | id | |
| spl set id | 1a143600-24b0-75dc-e063-6394a90afb53 | set_id |
Warnings cross-check#
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warnings
Warnings
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.