warnings
Warnings Keep out of reach of children. If pregnant or breast-feeding , ask a health professional before use.
Bach Original Flower Remedies Hornbeam
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
- Bach Original Flower Remedies Hornbeam
- Generic name
- CARPINUS BETULUS FLOWER
- Manufacturer
- Nelson Bach USA Limited
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 1a1d8183-b093-4a41-ba46-9b85861adb1d
- SPL ID
- ab51915e-e5eb-48b2-af59-22d533b719ca
- Version
- 3
- Effective date
- 2020-06-02
- Source export date
- 2026-09-28
- Source partition
- 9
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:01:02
| 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 | Bach Original Flower Remedies Hornbeam | openfda.brand_name | |
| generic name | CARPINUS BETULUS FLOWER | openfda.generic_name | |
| manufacturer name | Nelson Bach USA Limited | openfda.manufacturer_name | |
| ndc | package | 57687-266-20 | openfda.package_ndc |
| ndc | product | 57687-266 | openfda.product_ndc |
| ndc11 | package | 57687026620 | derived:openfda.package_ndc |
| spl id | ab51915e-e5eb-48b2-af59-22d533b719ca | id | |
| spl set id | 1a1d8183-b093-4a41-ba46-9b85861adb1d | set_id | |
| unii | 07YL55QKZ9 | 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.