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.
Gout 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
- Gout Symptom Relief
- Generic name
- AMMON PHOS, BELLADONNA, COLCHICUM AUTUMNALE, FORMICUM ACIDUM, FRAXINUS EXCELSIOR, LEDUM PALUSTRE, NATRUM CARBONICUM, NUX VOMICA AND URTICA URENS.
- Manufacturer
- King Bio Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 41dc03fc-169b-4691-bd62-9a41d7a6d2f7
- SPL ID
- 4590e343-960e-4fa7-888e-8b9ed5ad93bd
- Version
- 1
- Effective date
- 2026-03-06
- 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 02:17:41
| 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 | Gout Symptom Relief | openfda.brand_name | |
| generic name | AMMON PHOS, BELLADONNA, COLCHICUM AUTUMNALE, FORMICUM ACIDUM, FRAXINUS EXCELSIOR, LEDUM PALUSTRE, NATRUM CARBONICUM, NUX VOMICA AND URTICA URENS. | openfda.generic_name | |
| manufacturer name | King Bio Inc. | openfda.manufacturer_name | |
| ndc | package | 57955-9975-2 | openfda.package_ndc |
| ndc | product | 57955-9975 | openfda.product_ndc |
| ndc11 | package | 57955997502 | derived:openfda.package_ndc |
| spl id | 4590e343-960e-4fa7-888e-8b9ed5ad93bd | id | |
| spl set id | 41dc03fc-169b-4691-bd62-9a41d7a6d2f7 | set_id | |
| unii | 877L01IZ0P | openfda.unii | |
| unii | 0YIW783RG1 | openfda.unii | |
| unii | 269XH13919 | openfda.unii | |
| unii | 993QHL78E6 | openfda.unii | |
| unii | R6KCX5H8I2 | openfda.unii | |
| unii | 10LGE70FSU | openfda.unii | |
| unii | IHN2NQ5OF9 | openfda.unii | |
| unii | RC38362Q7M | openfda.unii | |
| unii | WQZ3G9PF0H | openfda.unii | |
| unii | 45P3261C7T | 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.