warnings
WARNINGS: If pregnant or breast feeding, consult a physician before use. Consult a health care provider for children under 12. Consult a physician if symptoms persist for more than 7 days. Keep out of reach of children.
THE FLOWER REMEDY Happy Heart
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
- THE FLOWER REMEDY Happy Heart
- Generic name
- GENTIANELLA AMARELLA, ULEX EUROPAEUS, ILEX AQUIFOLIUM, LONICERA CAPRIFOLIUM, SINAPIS ARVENSIS, ORNITHOGALUM UMBELLATUM, CASTANEA SATIVA, SALIX VITELLINA, IGNATIA AMARA, NATRUM MURIATICUM
- Manufacturer
- The Flower Remedy
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 6decd8fe-7593-4421-926c-f92400240032
- SPL ID
- 08d86895-720d-421e-8953-6227e09248fc
- Version
- 2
- Effective date
- 2025-12-03
- Source export date
- 2026-09-28
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:37:20
| 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 | THE FLOWER REMEDY Happy Heart | openfda.brand_name | |
| generic name | GENTIANELLA AMARELLA, ULEX EUROPAEUS, ILEX AQUIFOLIUM, LONICERA CAPRIFOLIUM, SINAPIS ARVENSIS, ORNITHOGALUM UMBELLATUM, CASTANEA SATIVA, SALIX VITELLINA, IGNATIA AMARA, NATRUM MURIATICUM | openfda.generic_name | |
| manufacturer name | The Flower Remedy | openfda.manufacturer_name | |
| ndc | package | 81183-103-30 | openfda.package_ndc |
| ndc | product | 81183-103 | openfda.product_ndc |
| ndc11 | package | 81183010330 | derived:openfda.package_ndc |
| spl id | 08d86895-720d-421e-8953-6227e09248fc | id | |
| spl set id | 6decd8fe-7593-4421-926c-f92400240032 | set_id | |
| unii | XBP5X7E70R | openfda.unii | |
| unii | 5ENR9SAN1W | openfda.unii | |
| unii | CZD6M4PY4B | openfda.unii | |
| unii | ZKH2SOY1AR | openfda.unii | |
| unii | 398DBS1PXN | openfda.unii | |
| unii | 451W47IQ8X | openfda.unii | |
| unii | 1NM3M2487K | openfda.unii | |
| unii | WWX61E1ZAK | openfda.unii | |
| unii | YHZ719F7M3 | openfda.unii | |
| unii | 1X0T378SXY | 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.