warnings
WARNINGS .
Childrens Multi Symptom Cold Very Berry
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 Multi Symptom Cold Very Berry
- Generic name
- DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL
- Manufacturer
- CVS
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 2a849ae9-338f-4642-e063-6394a90a1ca4
- SPL ID
- 7f613443-4706-4b26-a862-6ad6a7d7346b
- Version
- 2
- Effective date
- 2025-01-17
- Source export date
- 2026-10-12
- Source partition
- 5
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:44:26
| 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 Multi Symptom Cold Very Berry | openfda.brand_name | |
| generic name | DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | openfda.generic_name | |
| manufacturer name | CVS | openfda.manufacturer_name | |
| ndc | package | 51316-815-03 | openfda.package_ndc |
| ndc | product | 51316-815 | openfda.product_ndc |
| ndc11 | package | 51316081503 | derived:openfda.package_ndc |
| rxcui | 1043543 | openfda.rxcui | |
| spl id | 7f613443-4706-4b26-a862-6ad6a7d7346b | id | |
| spl set id | 2a849ae9-338f-4642-e063-6394a90a1ca4 | 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.