warnings
Warnings Stop use and consult a doctor if symptoms worsen or persist for more than 7 days. If pregnant or breast-feeding, ask a healthcare professional before use.
Restless Leg Symptom Relief
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
- Restless Leg Symptom Relief
- Generic name
- ARSENICUM ALBUM, BUFO RANA, CAUSTICUM, CHAMOMILLA, CROTALUS HORRIDUS, DIGITALIS PURPUREA, LACHESIS MUTUS, LILIUM TIGRINUM, PULSATILLA, RHUS TOX, SULPHUR, TARENTULA HISPANA, VISCUM ALBUM AND ZINCUM METALLICUM.
- Manufacturer
- King Bio Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 07ab09eb-9430-4ea2-90c0-db2ca237cc96
- SPL ID
- 3c58b3e2-9af9-4590-b9b7-7a8469e84140
- Version
- 1
- Effective date
- 2026-03-10
- Source export date
- 2026-10-12
- Source partition
- 14
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/acb9b4700b9af1bdda1c389c7b35bfe38fd6d1a62aa48d17832812be4029b84f/drug-label-0014-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 03:13:05
| 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 | Restless Leg Symptom Relief | openfda.brand_name | |
| generic name | ARSENICUM ALBUM, BUFO RANA, CAUSTICUM, CHAMOMILLA, CROTALUS HORRIDUS, DIGITALIS PURPUREA, LACHESIS MUTUS, LILIUM TIGRINUM, PULSATILLA, RHUS TOX, SULPHUR, TARENTULA HISPANA, VISCUM ALBUM AND ZINCUM METALLICUM. | openfda.generic_name | |
| manufacturer name | King Bio Inc. | openfda.manufacturer_name | |
| ndc | package | 57955-9970-2 | openfda.package_ndc |
| ndc | product | 57955-9970 | openfda.product_ndc |
| ndc11 | package | 57955997002 | derived:openfda.package_ndc |
| spl id | 3c58b3e2-9af9-4590-b9b7-7a8469e84140 | id | |
| spl set id | 07ab09eb-9430-4ea2-90c0-db2ca237cc96 | set_id | |
| unii | DD5FO1WKFU | openfda.unii | |
| unii | X67Z2963PI | openfda.unii | |
| unii | 6IO182RP7A | openfda.unii | |
| unii | S7V92P67HO | openfda.unii | |
| unii | Q59QU6N72Q | openfda.unii | |
| unii | 86M454L2TT | openfda.unii | |
| unii | 70FD1KFU70 | openfda.unii | |
| unii | VSW71SS07I | openfda.unii | |
| unii | BK9092J5MP | openfda.unii | |
| unii | F1T8QT9U8B | openfda.unii | |
| unii | YHA2XLJ956 | openfda.unii | |
| unii | G0R4UBI2ZZ | openfda.unii | |
| unii | J41CSQ7QDS | openfda.unii | |
| unii | I76KB35JEV | 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.