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.
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
- PULSATILLA, ALLIUM CEPA, ARSENICUM ALBUM, NUX VOMICA, EUPHRASIA OFFINALIS, SABADILLA, ARALIA RACEMOSA, CUPRUM METALLICUM
- Manufacturer
- Homeolab International (Canada) inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 7978fb75-fac9-480d-830c-c8c09ff29be1
- SPL ID
- 27e95caf-7afc-437c-b7c0-05f6df793fbc
- Version
- 1
- Effective date
- 2019-07-25
- Source export date
- 2026-10-30
- 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/2026-10-30/57469fe40e5b1c0d9604dc7dbc22532ea48e8e53acfb911fc676578d98492f7e/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 18:29:55
| 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 | PULSATILLA, ALLIUM CEPA, ARSENICUM ALBUM, NUX VOMICA, EUPHRASIA OFFINALIS, SABADILLA, ARALIA RACEMOSA, CUPRUM METALLICUM | openfda.generic_name | |
| manufacturer name | Homeolab International (Canada) inc | openfda.manufacturer_name | |
| ndc | package | 71971-9066-8 | openfda.package_ndc |
| ndc | product | 71971-9066 | openfda.product_ndc |
| ndc11 | package | 71971906608 | derived:openfda.package_ndc |
| spl id | 27e95caf-7afc-437c-b7c0-05f6df793fbc | id | |
| spl set id | 7978fb75-fac9-480d-830c-c8c09ff29be1 | set_id | |
| unii | C9642I91WL | openfda.unii | |
| unii | 789U1901C5 | openfda.unii | |
| unii | 269XH13919 | openfda.unii | |
| unii | T90W4582DU | openfda.unii | |
| unii | S7V92P67HO | openfda.unii | |
| unii | 6NAF1689IO | openfda.unii | |
| unii | 492225Q21H | openfda.unii | |
| unii | I76KB35JEV | 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.