warnings
Warnings Do not use if seal is broken or missing. Stop use and ask a doctor in cases of high fever or if symptoms worsen or persist for more than 3 days. Keep out of reach of children.
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
- ARSENICUM ALBUM, KALI PHOSPHORICUM, MERCURIS SOLUBILIS, NATRUM SULPHURICUM, HEPAR SULPHURIS CALCAREUM, ARUM TRIPHYLLUM
- Manufacturer
- Homeolab International (Canada) inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 18a6f6d4-cdfd-4bf7-8cb2-831033c1d965
- SPL ID
- bf3bb366-1d16-4aa8-b065-f66f22180b5b
- Version
- 1
- Effective date
- 2019-10-23
- Source export date
- 2026-10-12
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:29:56
| 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 | ARSENICUM ALBUM, KALI PHOSPHORICUM, MERCURIS SOLUBILIS, NATRUM SULPHURICUM, HEPAR SULPHURIS CALCAREUM, ARUM TRIPHYLLUM | openfda.generic_name | |
| manufacturer name | Homeolab International (Canada) inc | openfda.manufacturer_name | |
| ndc | package | 71971-9021-5 | openfda.package_ndc |
| ndc | package | 71971-9021-4 | openfda.package_ndc |
| ndc | package | 71971-9021-9 | openfda.package_ndc |
| ndc | product | 71971-9021 | openfda.product_ndc |
| ndc11 | package | 71971902109 | derived:openfda.package_ndc |
| ndc11 | package | 71971902104 | derived:openfda.package_ndc |
| ndc11 | package | 71971902105 | derived:openfda.package_ndc |
| spl id | bf3bb366-1d16-4aa8-b065-f66f22180b5b | id | |
| spl set id | 18a6f6d4-cdfd-4bf7-8cb2-831033c1d965 | set_id | |
| unii | CI71S98N1Z | openfda.unii | |
| unii | 324Y4038G2 | openfda.unii | |
| unii | 0YPR65R21J | openfda.unii | |
| unii | S7V92P67HO | openfda.unii | |
| unii | DM64K844DM | openfda.unii | |
| unii | 1MBW07J51Q | 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.