FDA.reportPublic FDA data

THE GOO

Manufacturer
APSM PERFORMANCE, LLC
Effective date
2026-01-23
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:34:43

Label at a glance#

ProductTHE GOO MEDICATED PAIN RELIEF
Active ingredientMETHYL SALICYLATE, MENTHOL, UNSPECIFIED FORM, CAMPHOR OIL
Label structure8 sections

Indications and uses

Temporary relief of minor aches and pains of muscles and joints associated with arthritis, backache, strain, sprains, and bruises.

Dosage and administration

Adults and children over 12: Apply a thin layer and massage into painful area until thoroughly absorbed. Repeat as necessary, but no more than 4 times daily. After applying, wash hands with soap and water. Children under 12: Ask a doctor.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Methyl Salicylate 30%

Menthol 10%

Camphor 4%

PURPOSE

OTC - PURPOSE SECTION

TOPICAL PAIN RELIEF

USES

INDICATIONS & USAGE SECTION

Temporary relief of minor aches and pains of muscles and joints associated with arthritis, backache, strain, sprains, and bruises.

WARNINGS

WARNINGS SECTION

Avoid contact with eyes. If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few
days, discontinue use of this product and consult a doctor. Do not use in large quantities, particularly over raw surfaces or blistered areas.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

1,2-Hexanediol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Caprylhydroxamic Acid, Capryloyl Glycerin/Sebacic Acid Copolymer, Dimethyl Isosorbide, Menthyl Ethylamido Oxalate, Propanediol, Steareth-2, Steareth-21, Stearyl Alcohol, Stearyl Glycyrrhetinate, Vanillyl Butyl Ether, Water, Xanthan Gum, Blue 1, Yellow 5, Green 3

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Adults and children over 12: Apply a thin layer and massage into painful area until thoroughly absorbed. Repeat as necessary, but no more than 4 times daily. After applying, wash hands with soap and water. Children under 12: Ask a doctor.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_The Goo_100mL01b LBL_The Goo_100mL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1116730camphor 4 % / menthol 10 % / methyl salicylate 30 % Topical GelPSN3
1116730camphor 0.04 MG/MG / menthol 0.1 MG/MG / methyl salicylate 0.3 MG/MG Topical GelSCD3
1116730camphor 4 % / menthol 10 % / methyl salicylate 30 % Topical GelSY3

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130636628061118GTIN-13: 0636628061118
EAN-13: 0636628061118
GTIN-12: 636628061118
UPC-A: 636628061118
GTIN storage (14 digits): 00636628061118		01b LBL_The Goo_100mL.jpg
QR code linkQR Codeqrco.de/bcfCGo01b LBL_The Goo_100mL.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82503-101-11THE GOOMEDICATED PAIN RELIEF100 mL in 1 BOTTLEGEL1003

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82503-10182503-101-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S)N7YC58165TIACT
XANTHAN GUMTTV12P4NEEIACT
CAPRYLHYDROXAMIC ACIDUPY805K99WIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
PROPANEDIOL5965N8W85TIACT
DIMETHYL ISOSORBIDESA6A6V432SIACT
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED)809Y72KV36IACT
STEARYL GLYCYRRHETINATE3YYE6VJS0PIACT
FD&C YELLOW NO. 5 FREE ACID6TP696149NIACT
FD&C GREEN NO. 33P3ONR6O1SIACT
STEARETH-2V56DFE46J5IACT
FD&C BLUE NO. 1H3R47K3TBDIACT
WATER059QF0KO0RIACT
STEARETH-2153J3F32P58IACT
STEARYL ALCOHOL2KR89I4H1YIACT
MENTHYL ETHYLAMIDO OXALATEG2MB8B7PSMIACT
VANILLYL BUTYL ETHERS2ULN37C9RIACT
SODIUM HYDROXIDE55X04QC32IIACT
METHYL SALICYLATELAV5U5022YACTIB
MENTHOL, UNSPECIFIED FORML7T10EIP3AACTIB
CAMPHOR OIL75IZZ8Y727ACTIB

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
THE GOO MEDICATED PAIN RELIEFMETHYL SALICYLATE, MENTHOL, CAMPHORAPSM PERFORMANCE, LLCdb4c321c-8cdc-5a11-e053-2995a90a91a12026-01-23WarningsExact identifier
ndc (package): 82503-101-11
ndc (product): 82503-101
ndc11 (package): 82503010111
spl id: 4914f51b-96e4-989e-e063-6394a90a424f
spl set id: db4c321c-8cdc-5a11-e053-2995a90a91a1

Reported adverse events (FAERS/openFDA)#

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