warnings
Warnings Stop use and ask a doctor in cases of hgh 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
- PULSATILLA, ALLIUM CEPA, ARSENICUM ALBUM, NUX VOMICA, EUPHRASIA OFFINALIS, SABADILLA, STICTA PULMONARIA, ARAILA RACEMOSA, CUPRUM METALLICUM
- Manufacturer
- Homeolab International (Canada) inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- ba120c26-1e84-48b9-b38a-df5aa75ea6ce
- SPL ID
- 89e04889-f92f-41d0-9e45-a5eddb46453f
- Version
- 2
- Effective date
- 2019-07-16
- Source export date
- 2026-11-06
- 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/2026-11-06/b0d9ca61dc485ebaf55e14a76d7d677668e40ef1e1978cdbcc4d73d58eba0b99/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 07:46:05
| 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, STICTA PULMONARIA, ARAILA RACEMOSA, CUPRUM METALLICUM | openfda.generic_name | |
| manufacturer name | Homeolab International (Canada) inc | openfda.manufacturer_name | |
| ndc | package | 71971-9077-8 | openfda.package_ndc |
| ndc | product | 71971-9077 | openfda.product_ndc |
| ndc11 | package | 71971907708 | derived:openfda.package_ndc |
| spl id | 89e04889-f92f-41d0-9e45-a5eddb46453f | id | |
| spl set id | ba120c26-1e84-48b9-b38a-df5aa75ea6ce | 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 | |
| unii | D1YM0P5Z2T | 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.