FDA.reportPublic FDA data

Arthritis Wonder

Manufacturer
G2 Products LLC
Effective date
2020-03-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:05:03

Label at a glance#

ProductArthritis Wonder
Active ingredientMENTHOL
Label structure7 sections

Indications and uses

For the temporary relief of minor aches and pains of muscles and joints associated with ● arthritis ● simple backache ● strains ● bruises ● sprains

Dosage and administration

• Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily • Children under 2 years of age: consult a doctor

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 1.25%

Purpose

OTC - PURPOSE SECTION

External analgesic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints associated with ● arthritis ● simple backache ● strains ● bruises ● sprains

Warnings

WARNINGS SECTION

For external use only.

Flammable: Keep away from fire or flame.

When using this product

OTC - WHEN USING SECTION

• avoid contact with the eyes • do not bandage tightly

Do not use

OTC - DO NOT USE SECTION

● on wounds or damaged skin with a heating pad

Stop use and ask a doctor if

OTC - STOP USE SECTION

• condition worsens • symptoms persist for more than 7 days • symptoms clear up and occur again within a few days

Keep out of the reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away

Directions

INSTRUCTIONS FOR USE SECTION

• Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily • Children under 2 years of age: consult a doctor

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Juice, Butylene Glycol, Caprylic/Capric Triglyceride, Caprylyl Glycol, Ceteareth-20, Cetearyl Alcohol, Dimethicone, Dimethyl Sulfone, Ethoxydiglycol, Ethylhexylglycerin, Glycerin, Glyceryl Stearate, Hexylene Glycol, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Mentha Piperita (Peppermint) Oil, PEG-100 Stearate, Phenoxyethanol, Polysorbate 60, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Sorbitan Isostearate, Squalane, Stearic Acid, Tetrasodium Glutamate Diacetate, Water, Wogonin, Xanthan Gum

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display PanelPrincipal Display Panel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
416982menthol 1.25 % Topical CreamPSN1
416982menthol 12.5 MG/ML Topical CreamSCD1
416982menthol 1.25 % Topical CreamSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71893-101-112022-01-28C16284748780-1d6a99b39-6e15-a426-e053-dadaa90af4c2Arthritis Wonder

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71893-101-11Arthritis Wonder226 g in 1 TUBECREAM2261

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71893-101ARTHRITIS WONDER (MENTHOL) CREAM [G2 PRODUCTS LLC]1Legacy NDC, 1 package rows20200406_a1ced32a-07fd-cbc3-e053-2995a90a529f.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 30 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71893-10171893-101-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 28 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIMETHICONE92RU3N3Y1OIACT
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%)86FQE96TZ4IACT
PEG-100 STEARATEYD01N1999RIACT
PHENOXYETHANOLHIE492ZZ3TIACT
DIETHYLENE GLYCOL MONOETHYL ETHERA1A1I8X02BIACT
GLYCERINPDC6A3C0OXIACT
HEXYLENE GLYCOLKEH0A3F75JIACT
PEPPERMINT OILAV092KU4JHIACT
POLYSORBATE 60CAL22UVI4MIACT
SORBITAN ISOSTEARATE01S2G2C1E4IACT
TETRASODIUM GLUTAMATE DIACETATE5EHL50I4MYIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
WATER059QF0KO0RIACT
WOGONINPOK93PO28WIACT
XANTHAN GUMTTV12P4NEEIACT
CARBOMER INTERPOLYMER TYPE A (55000 CPS)59TL3WG5COIACT
ALOE VERA LEAFZY81Z83H0XIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
CAPRYLYL GLYCOL00YIU5438UIACT
POLYOXYL 20 CETOSTEARYL ETHERYRC528SWUYIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
DIMETHYL SULFONE9H4PO4Z4FTIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
ALMOND OIL66YXD4DKO9IACT
SQUALANEGW89575KF9IACT
STEARIC ACID4ELV7Z65APIACT
MENTHOLL7T10EIP3AACTIB

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
a1ceea19-4af1-128b-e053-2995a90a697ca1ced32a-07fd-cbc3-e053-2995a90a529f2020-03-26WarningsExact identifier
spl id: a1ceea19-4af1-128b-e053-2995a90a697c
spl set id: a1ced32a-07fd-cbc3-e053-2995a90a529f

Reported adverse events (FAERS/openFDA)#

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