warnings
Warnings: If symptoms persist or worsen, or if pregnant or nursing, consult a doctor. Keep out of reach of children. Do not use if cap seal is broken or missing.
Sciatica 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
- Sciatica Relief
- Generic name
- ARNICA MONTANA FLOWER, BRYONIA ALBA WHOLE, MATRICARIA RECUTITA, PSEUDOGNAPHALIUM LUTEOALBUM LEAF, KALMIA LATIFOLIA LEAF, TOXICODENDRON PUBESCENS LEAF, VISCUM ALBUM LEAF
- Manufacturer
- Homeocare Laboratories
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 5fbffd54-0007-4b9b-922f-1c0e450abd55
- SPL ID
- 7e58d660-4924-5cab-e053-2a91aa0ac70f
- Version
- 2
- Effective date
- 2018-12-31
- Source export date
- 2026-10-27
- 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/2026-10-27/977776a6cc37ec1c77259da8a93ae161850a3aa120341096e5a03428b84d016b/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:59:54
| Harmonized routes |
|---|
| SUBLINGUAL |
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 | Sciatica Relief | openfda.brand_name | |
| generic name | ARNICA MONTANA FLOWER, BRYONIA ALBA WHOLE, MATRICARIA RECUTITA, PSEUDOGNAPHALIUM LUTEOALBUM LEAF, KALMIA LATIFOLIA LEAF, TOXICODENDRON PUBESCENS LEAF, VISCUM ALBUM LEAF | openfda.generic_name | |
| manufacturer name | Homeocare Laboratories | openfda.manufacturer_name | |
| ndc | package | 61727-323-21 | openfda.package_ndc |
| ndc | product | 61727-323 | openfda.product_ndc |
| ndc11 | package | 61727032321 | derived:openfda.package_ndc |
| spl id | 7e58d660-4924-5cab-e053-2a91aa0ac70f | id | |
| spl set id | 5fbffd54-0007-4b9b-922f-1c0e450abd55 | set_id | |
| unii | GN8217WQOV | openfda.unii | |
| unii | XK4IUX8MNB | openfda.unii | |
| unii | 79N6542N18 | openfda.unii | |
| unii | 6IO182RP7A | openfda.unii | |
| unii | BGI20Z6M57 | openfda.unii | |
| unii | OZ0E5Y15PZ | openfda.unii | |
| unii | 56K0VVT47P | openfda.unii | |
| unii | G0R4UBI2ZZ | 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.