warnings
Warnings Stop use and ask a doctor if difficulty breathing, vomiting, skin rash, diarrhea or fever above 100º F (38ºC) develops symptoms persist for more than 2 days or worsen Keep out of reach of children.
Childrens Cold Crush
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 Cold Crush
- Generic name
- ACONITUM NAPELLUS, ALLIUM CEPA, BRYONIA ALBA, CHAMOMILLA, ECHINACEA ANGUSTIFOLIA, EUPHRASIA OFFICINALIS, GELSEMIUM SEMPERVIRENS, IPECACUANHA, PULSATILLA, SAMBUCUS NIGRA
- Manufacturer
- Genexa Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 32ece9d6-b346-6304-e063-6394a90a182d
- SPL ID
- 32ece9d6-b347-6304-e063-6394a90a182d
- Version
- 1
- Effective date
- 2025-04-16
- Source export date
- 2026-09-28
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:15:23
| 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 |
|---|---|---|---|
| brand name | Childrens Cold Crush | openfda.brand_name | |
| generic name | ACONITUM NAPELLUS, ALLIUM CEPA, BRYONIA ALBA, CHAMOMILLA, ECHINACEA ANGUSTIFOLIA, EUPHRASIA OFFICINALIS, GELSEMIUM SEMPERVIRENS, IPECACUANHA, PULSATILLA, SAMBUCUS NIGRA | openfda.generic_name | |
| manufacturer name | Genexa Inc. | openfda.manufacturer_name | |
| ndc | package | 69676-0073-1 | openfda.package_ndc |
| ndc | product | 69676-0073 | openfda.product_ndc |
| ndc11 | package | 69676007301 | derived:openfda.package_ndc |
| spl id | 32ece9d6-b347-6304-e063-6394a90a182d | id | |
| spl set id | 32ece9d6-b346-6304-e063-6394a90a182d | set_id | |
| unii | C9642I91WL | openfda.unii | |
| unii | 639KR60Q1Q | openfda.unii | |
| unii | VB06AV5US8 | openfda.unii | |
| unii | 492225Q21H | openfda.unii | |
| unii | 8E272251DI | openfda.unii | |
| unii | 62I3C8233L | openfda.unii | |
| unii | T7J046YI2B | openfda.unii | |
| unii | U0NQ8555JD | openfda.unii | |
| unii | G0R4UBI2ZZ | openfda.unii | |
| unii | 07V4DX094T | 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.