warnings
WARNINGS Consult a physician for use in children under 6 years of age. Contact a doctor if symptoms persist.
Recover Ease Trauma - Pain
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
- Recover Ease Trauma - Pain
- Generic name
- ARNICA MONTANA 9CH, BELLIS PERENNIS 5CH, BRYONIA 9CH, CALENDULA OFFICINALIS 5CH, HYPERICUM PERFORATUM 5CH, RHUS TOXICODENDRON 9CH, RUTA GRAVEOLENS 5CH
- Manufacturer
- SEVENE USA
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 54844b24-0704-b7eb-e063-6394a90a359d
- SPL ID
- 594f629b-ee7e-9a45-e063-6294a90af4da
- Version
- 3
- Effective date
- 2026-08-18
- Source export date
- 2026-09-28
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:28:29
| Harmonized routes |
|---|
| BUCCAL |
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 | Recover Ease Trauma - Pain | openfda.brand_name | |
| generic name | ARNICA MONTANA 9CH, BELLIS PERENNIS 5CH, BRYONIA 9CH, CALENDULA OFFICINALIS 5CH, HYPERICUM PERFORATUM 5CH, RHUS TOXICODENDRON 9CH, RUTA GRAVEOLENS 5CH | openfda.generic_name | |
| manufacturer name | SEVENE USA | openfda.manufacturer_name | |
| ndc | package | 76472-7000-2 | openfda.package_ndc |
| ndc | package | 76472-7000-1 | openfda.package_ndc |
| ndc | product | 76472-7000 | openfda.product_ndc |
| ndc11 | package | 76472700001 | derived:openfda.package_ndc |
| ndc11 | package | 76472700002 | derived:openfda.package_ndc |
| spl id | 594f629b-ee7e-9a45-e063-6294a90af4da | id | |
| spl set id | 54844b24-0704-b7eb-e063-6394a90a359d | set_id | |
| unii | XK4IUX8MNB | openfda.unii | |
| unii | CDH3461U7L | openfda.unii | |
| unii | O80TY208ZW | openfda.unii | |
| unii | 18E7415PXQ | openfda.unii | |
| unii | 2HU33I03UY | openfda.unii | |
| unii | N94C2U587S | openfda.unii | |
| unii | 53UB5FH7CX | 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.