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
- Homeolab International (Canada) inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- ce7273d4-01f8-4b6b-b33a-83bd2d4fb07a
- SPL ID
- 93a1a99e-bfd0-4818-92b9-b64f2c775f05
- Version
- 3
- Effective date
- 2019-12-10
- Source export date
- 2026-10-12
- 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/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:45:00
| 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 | Homeolab International (Canada) inc | openfda.manufacturer_name | |
| ndc | package | 71971-9104-9 | openfda.package_ndc |
| ndc | package | 71971-9104-4 | openfda.package_ndc |
| ndc | package | 71971-9104-5 | openfda.package_ndc |
| ndc | product | 71971-9104 | openfda.product_ndc |
| ndc11 | package | 71971910405 | derived:openfda.package_ndc |
| ndc11 | package | 71971910409 | derived:openfda.package_ndc |
| ndc11 | package | 71971910404 | derived:openfda.package_ndc |
| spl id | 93a1a99e-bfd0-4818-92b9-b64f2c775f05 | id | |
| spl set id | ce7273d4-01f8-4b6b-b33a-83bd2d4fb07a | 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.