warnings
WARNINGS: • If pregnant or breastfeeding, ask a health professional before use. • Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
Relaxing Legs
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
- Relaxing Legs
- Generic name
- ACONITUM NAPELLUS, GNAPHALIUM POLYCEPHALUM, LEDUM PALUSTRE, MAGNESIA PHOSPHORICA, RHUS TOX, VISCUM ALBUM
- Manufacturer
- The Magni Company
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 800257d9-c0fb-4c71-a2c7-20602523e4ac
- SPL ID
- 03549715-f48c-4fc5-a824-2725dfea3f47
- Version
- 5
- Effective date
- 2024-02-08
- Source export date
- 2026-10-12
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:17:00
| 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 | Relaxing Legs | openfda.brand_name | |
| generic name | ACONITUM NAPELLUS, GNAPHALIUM POLYCEPHALUM, LEDUM PALUSTRE, MAGNESIA PHOSPHORICA, RHUS TOX, VISCUM ALBUM | openfda.generic_name | |
| manufacturer name | The Magni Company | openfda.manufacturer_name | |
| ndc | package | 43689-0021-1 | openfda.package_ndc |
| ndc | package | 43689-0021-2 | openfda.package_ndc |
| ndc | product | 43689-0021 | openfda.product_ndc |
| ndc11 | package | 43689002101 | derived:openfda.package_ndc |
| ndc11 | package | 43689002102 | derived:openfda.package_ndc |
| spl id | 03549715-f48c-4fc5-a824-2725dfea3f47 | id | |
| spl set id | 800257d9-c0fb-4c71-a2c7-20602523e4ac | set_id | |
| unii | 877L01IZ0P | openfda.unii | |
| unii | HF539G9L3Q | openfda.unii | |
| unii | 6IO182RP7A | openfda.unii | |
| unii | 36XQ854NWW | openfda.unii | |
| unii | U0NQ8555JD | openfda.unii | |
| unii | BK9092J5MP | 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.