warnings
Warnings • A PHYSICIAN SHOULD ALWAYS BE CONSULTED TO RULE OUT SERIOUS CAUSES. • This product is intended to complement, not replace, standard medical treatment. • Initial worsening of symptoms may occur.
Fibromyalgia 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
- Fibromyalgia Relief
- Generic name
- BRYONIA ALBA ROOT - CAUSTICUM - LOESELIA MEXICANA WHOLE - MAGNESIUM PHOSPHATE - PULSATILLA VULGARIS - TOXICODENDRON PUBESCENS LEAF - VALERIAN
- Manufacturer
- TRP Company
- Product type
- HUMAN OTC DRUG
- SPL set ID
- a6ba3058-ec39-715f-e053-2995a90aa32a
- SPL ID
- 4604abd2-4b86-95d9-e063-6394a90a60d8
- Version
- 4
- Effective date
- 2025-12-15
- Source export date
- 2026-09-28
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:37:12
| 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 | Fibromyalgia Relief | openfda.brand_name | |
| generic name | BRYONIA ALBA ROOT - CAUSTICUM - LOESELIA MEXICANA WHOLE - MAGNESIUM PHOSPHATE - PULSATILLA VULGARIS - TOXICODENDRON PUBESCENS LEAF - VALERIAN | openfda.generic_name | |
| manufacturer name | TRP Company | openfda.manufacturer_name | |
| ndc | package | 17312-171-14 | openfda.package_ndc |
| ndc | product | 17312-171 | openfda.product_ndc |
| ndc11 | package | 17312017114 | derived:openfda.package_ndc |
| spl id | 4604abd2-4b86-95d9-e063-6394a90a60d8 | id | |
| spl set id | a6ba3058-ec39-715f-e053-2995a90aa32a | set_id | |
| unii | DD5FO1WKFU | openfda.unii | |
| unii | HF539G9L3Q | openfda.unii | |
| unii | 6IO182RP7A | openfda.unii | |
| unii | T7J046YI2B | openfda.unii | |
| unii | I76KB35JEV | openfda.unii | |
| unii | XA8YCV5M3E | 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.