Home DailyMed 3f9ce9b8-1e50-5fb2-e054-00144ff88e88 Gout Reliever Synergy Drug label information. FDA.report displays public Structured Product Labeling data from DailyMed and legacy FDA.report DailyMed cache rows. This page is not medical advice, prescribing advice, or a substitute for the official label reviewed by a qualified healthcare professional. Labeling can change; when a current hydrated DailyMed SPL record is available, FDA.report shows that newer record before legacy cached files.
Manufacturer PHYTOPIA CO., LTD.
Effective date 2016-10-24
Label type HUMAN OTC DRUG LABEL
Version 1
Source full-release
Hydrated at 2026-05-31 22:47:44 Label at a glance# Product Gout Reliever Synergy
Active ingredient MENTHOL
Label structure 5 sections
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70470-1113-5 Gout Reliever Synergy 500 mg in 1 BOTTLE, GLASS OIL 500 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70470-1113 GOUT RELIEVER SYNERGY OIL [PHYTOPIA CO., LTD.] 1 1 package rows 20161024_3f9ce9b8-1e50-5fb2-e054-00144ff88e88.zip
Products# Every source-derived product name is available through these pages.
DailyMed product names page 1 of 1 · 11 matching rows.
Gout Reliever Synergy MENTHOL JUNIPER BERRY OIL MATRICARIA RECUTITA ARNICA MONTANA BORAGE OIL GAULTHERIA PROCUMBENS LEAF PEPPERMINT OIL GRAPEFRUIT OIL EUCALYPTUS OIL OLIVE OIL Ingredients# Every source-derived ingredient row is available through these pages.
DailyMed ingredient rows page 1 of 1 · 10 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.