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 Get Up and Go
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 Get Up and Go
- Generic name
- GENTIANELLA AMARELLA, ULEX EUROPAEUS, LARIX DECIDUA, QUERCUS ROBUR, OLEA EUROPAEA, CASTANEA SATIVA, BROMUS RAMOSUS, CARBO VEGETABILIS
- Manufacturer
- The Flower Remedy
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 52171aaa-8154-46c4-a807-7a7d209aa6cc
- SPL ID
- f8fa5592-f48c-4d9d-b10e-fabb873d400d
- Version
- 2
- Effective date
- 2025-12-03
- Source export date
- 2026-10-12
- 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/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:28:10
| 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 Get Up and Go | openfda.brand_name | |
| generic name | GENTIANELLA AMARELLA, ULEX EUROPAEUS, LARIX DECIDUA, QUERCUS ROBUR, OLEA EUROPAEA, CASTANEA SATIVA, BROMUS RAMOSUS, CARBO VEGETABILIS | openfda.generic_name | |
| manufacturer name | The Flower Remedy | openfda.manufacturer_name | |
| ndc | package | 81183-102-30 | openfda.package_ndc |
| ndc | product | 81183-102 | openfda.product_ndc |
| ndc11 | package | 81183010230 | derived:openfda.package_ndc |
| spl id | f8fa5592-f48c-4d9d-b10e-fabb873d400d | id | |
| spl set id | 52171aaa-8154-46c4-a807-7a7d209aa6cc | set_id | |
| unii | 2P3VWU3H10 | openfda.unii | |
| unii | 9UMZ642257 | openfda.unii | |
| unii | ZKH2SOY1AR | openfda.unii | |
| unii | 398DBS1PXN | openfda.unii | |
| unii | ML644HED2V | openfda.unii | |
| unii | YHZ719F7M3 | openfda.unii | |
| unii | 498M34P1VZ | openfda.unii | |
| unii | 0W9O574LE8 | 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.