warnings
Warnings • For external use only • Avoid contact with eyes Keep out of reach of children • If symptoms persist for more than 7 days or worsen, consult your physician Do not use • on open wounds cuts, damaged, or infected skin
Magnilife Pain Relieving Foot
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
- Magnilife Pain Relieving Foot
- Generic name
- APIS MELLIFERA, LEONTOPODIUM NIVALE SUBSP. ALPINUM WHOLE, SULFUR
- Manufacturer
- The Magni Group, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 626e52cc-3031-47a4-8e31-f5ae51b51846
- SPL ID
- 558ffcf7-b07f-d924-e063-6394a90a5c8b
- Version
- 1
- Effective date
- 2026-07-01
- Source export date
- 2026-09-28
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:19:50
| Harmonized routes |
|---|
| TOPICAL |
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 | Magnilife Pain Relieving Foot | openfda.brand_name | |
| generic name | APIS MELLIFERA, LEONTOPODIUM NIVALE SUBSP. ALPINUM WHOLE, SULFUR | openfda.generic_name | |
| manufacturer name | The Magni Group, Inc. | openfda.manufacturer_name | |
| ndc | package | 43689-0063-2 | openfda.package_ndc |
| ndc | package | 43689-0063-1 | openfda.package_ndc |
| ndc | product | 43689-0063 | openfda.product_ndc |
| ndc11 | package | 43689006301 | derived:openfda.package_ndc |
| ndc11 | package | 43689006302 | derived:openfda.package_ndc |
| spl id | 558ffcf7-b07f-d924-e063-6394a90a5c8b | id | |
| spl set id | 626e52cc-3031-47a4-8e31-f5ae51b51846 | set_id | |
| unii | 7R4LQP52DM | openfda.unii | |
| unii | 70FD1KFU70 | openfda.unii | |
| unii | 7S82P3R43Z | 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.