warnings
Warnings Do not use if bottle 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 2 days.
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
- COLOCYNTHIS, MAGNESIA PHOSPHORICA, CHAMOMILLA, DIOSCOREA VILLOSA
- Manufacturer
- Homeolab International (Canada) inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- df8e8995-3106-4b21-acc4-24eeefd109fc
- SPL ID
- 3c6169c7-d8f8-4cbe-adf3-efedd55bc0ee
- Version
- 2
- Effective date
- 2019-07-16
- Source export date
- 2026-09-28
- 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/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:07:15
| 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 | COLOCYNTHIS, MAGNESIA PHOSPHORICA, CHAMOMILLA, DIOSCOREA VILLOSA | openfda.generic_name | |
| manufacturer name | Homeolab International (Canada) inc | openfda.manufacturer_name | |
| ndc | package | 71971-9083-8 | openfda.package_ndc |
| ndc | product | 71971-9083 | openfda.product_ndc |
| ndc11 | package | 71971908308 | derived:openfda.package_ndc |
| spl id | 3c6169c7-d8f8-4cbe-adf3-efedd55bc0ee | id | |
| spl set id | df8e8995-3106-4b21-acc4-24eeefd109fc | set_id | |
| unii | IWY3IWX2G8 | openfda.unii | |
| unii | HF539G9L3Q | openfda.unii | |
| unii | G0R4UBI2ZZ | openfda.unii | |
| unii | 23H32AOH17 | 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.