FDA.reportPublic FDA data

Gout Relief 3310A Plus

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 (canonical bytes are SHA-256 checked before publication)

Brand name
Gout Relief 3310A Plus
Generic name
GOUT RELIEF 3310A PLUS
Manufacturer
Bispit Canada Ltd.
Product type
HUMAN OTC DRUG
SPL set ID
3e0a4e26-61b6-01cb-e063-6294a90a4efc
SPL ID
3e1d060f-1584-3b66-e063-6394a90a5996
Version
2
Effective date
2025-09-06
Source export date
2026-09-28
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:07:20
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Ulsing three bottles is generally effective fordissolving crystals (as crystal dissoiution takestime); You should experience noticeable effects afterat least 21 days of conbnlous use,It is noral to experence increose in uric acidlevels or gout recurrencelchanges imn affectedareas during the early days of use;Refrain from olcohol consumption, or limit itsionificantly, for at least 15 days before takingthis product; lt has an auxiliary effect on improving libidoand supporting prostate health, Do not use if you have a seafood allergy. Store properly and out of reach of children.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.