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 Peaceful Night
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 Peaceful Night
- Generic name
- PRUNUS CERASIFERA, CLEMATIS VITALBA, ULMUS PROCERA, IMPATIENS GLANDULIFERA, QUERCUS ROBUR, HELIANTHEMUM NUMMULARIUM, AESCULUS HIPPOCASTANUM, IGNATIA AMARA
- Manufacturer
- The Flower Remedy
- Product type
- HUMAN OTC DRUG
- SPL set ID
- a0f2b6db-62a4-43b7-88f2-09b2a3c567de
- SPL ID
- 98e0c38e-1c39-4bb6-ac67-e3afe68aaf8c
- Version
- 2
- Effective date
- 2025-12-03
- Source export date
- 2026-09-28
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:19:35
| 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 Peaceful Night | openfda.brand_name | |
| generic name | PRUNUS CERASIFERA, CLEMATIS VITALBA, ULMUS PROCERA, IMPATIENS GLANDULIFERA, QUERCUS ROBUR, HELIANTHEMUM NUMMULARIUM, AESCULUS HIPPOCASTANUM, IGNATIA AMARA | openfda.generic_name | |
| manufacturer name | The Flower Remedy | openfda.manufacturer_name | |
| ndc | package | 81183-101-30 | openfda.package_ndc |
| ndc | product | 81183-101 | openfda.product_ndc |
| ndc11 | package | 81183010130 | derived:openfda.package_ndc |
| spl id | 98e0c38e-1c39-4bb6-ac67-e3afe68aaf8c | id | |
| spl set id | a0f2b6db-62a4-43b7-88f2-09b2a3c567de | set_id | |
| unii | 0KD7R09EAS | openfda.unii | |
| unii | 7SCP4N87CI | openfda.unii | |
| unii | KK0Z92II8M | openfda.unii | |
| unii | 1NM3M2487K | openfda.unii | |
| unii | 51BRR32WPP | openfda.unii | |
| unii | AJU5O1A5ZV | openfda.unii | |
| unii | ML644HED2V | openfda.unii | |
| unii | J3O020I532 | 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.