Gout Reliever Synergy

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#

ProductGout Reliever Synergy
Active ingredientMENTHOL
Label structure5 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Drug facts

Methyl salicylate 50mg

Menthol 20mg

Analgesic in the treatment of gout pain. Helps relieve the condition of pain and stiffness.

OTC - PURPOSE SECTION

Drug facts

Methyl salicylate 50mg

Menthol 20mg

Analgesic in the treatment of gout pain. Helps relieve the condition of pain and stiffness.

DOSAGE & ADMINISTRATION SECTION

Dosage and Usage

Adults 5ml maximum per day

Apply on skin and gentle massage around painful area.

INDICATIONS & USAGE SECTION

Dosage and Usage

Adults 5ml maximum per day

Apply on skin and gentle massage around painful area.

INACTIVE INGREDIENT SECTION

Other ingredients

Arnica montana, peppermint, olive oil, grapefruit oil, eucalyptus oil, matricaria recutita, juniper berry oil, borage oil

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Warnings

For external use only. Stop use and ask doctor if rash occurs. Keep out reach of children. Protect this product from excessive heat and direct sun.

WARNINGS SECTION

Warnings

For external use only. Stop use and ask doctor if rash occurs. Keep out reach of children. Protect this product from excessive heat and direct sun.

STORAGE AND HANDLING SECTION

Warnings

For external use only. Stop use and ask doctor if rash occurs. Keep out reach of children. Protect this product from excessive heat and direct sun.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Gout reliever synergyGout reliever synergy

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70470-1113-52020-01-31C16284748780-19d75b9d0-e5e4-f424-e053-dadaa90a57ce3f9ce9b8-1e50-5fb2-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70470-1113-5Gout Reliever Synergy500 mg in 1 BOTTLE, GLASSOIL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70470-1113GOUT RELIEVER SYNERGY OIL [PHYTOPIA CO., LTD.]11 package rows20161024_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.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70470-111370470-1113-5

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML

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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
3f9ce9b8-1e51-5fb2-e054-00144ff88e883f9ce9b8-1e50-5fb2-e054-00144ff88e882016-10-24WarningsExact identifier
spl id: 3f9ce9b8-1e51-5fb2-e054-00144ff88e88
spl set id: 3f9ce9b8-1e50-5fb2-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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