warnings
Warnings Stop use and ask a doctor if symptoms worsen.
Kids Relief
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
- Kids Relief
- Generic name
- ASAFOETIDA, IGNATIA AMARA, VALERIANA OFFICINALIS, AVENA SATIVA, ARGENTUM NITRICUM, HYOSCYAMUS NIGER, PAEONIA OFFICINALIS, STRAMONIUM, COCCULUS INDICUS
- Manufacturer
- Laboratoire Atlas Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- fdc34e7c-1611-4aa0-a93a-7123644767a0
- SPL ID
- 40aac5cc-1af5-a4d9-e063-6394a90a89fc
- Version
- 9
- Effective date
- 2025-10-08
- Source export date
- 2026-09-28
- Source partition
- 14
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:40:56
| 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 | Kids Relief | openfda.brand_name | |
| generic name | ASAFOETIDA, IGNATIA AMARA, VALERIANA OFFICINALIS, AVENA SATIVA, ARGENTUM NITRICUM, HYOSCYAMUS NIGER, PAEONIA OFFICINALIS, STRAMONIUM, COCCULUS INDICUS | openfda.generic_name | |
| manufacturer name | Laboratoire Atlas Inc | openfda.manufacturer_name | |
| ndc | package | 63388-910-49 | openfda.package_ndc |
| ndc | package | 63388-910-44 | openfda.package_ndc |
| ndc | package | 63388-910-45 | openfda.package_ndc |
| ndc | product | 63388-910 | openfda.product_ndc |
| ndc11 | package | 63388091049 | derived:openfda.package_ndc |
| ndc11 | package | 63388091044 | derived:openfda.package_ndc |
| ndc11 | package | 63388091045 | derived:openfda.package_ndc |
| spl id | 40aac5cc-1af5-a4d9-e063-6394a90a89fc | id | |
| spl set id | fdc34e7c-1611-4aa0-a93a-7123644767a0 | set_id | |
| unii | 8R564U2E1P | openfda.unii | |
| unii | 95IT3W8JZE | openfda.unii | |
| unii | W9FZA51AS1 | openfda.unii | |
| unii | 1NM3M2487K | openfda.unii | |
| unii | FP6O7F1X9R | openfda.unii | |
| unii | 4WRK2153H3 | openfda.unii | |
| unii | KQX236OK4U | openfda.unii | |
| unii | 8O4P2U3QO2 | openfda.unii | |
| unii | G6W4F0V8Z3 | 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.