Active Ingredients
Methyl Salicylate 30%
Menthol 10%
Camphor 4%
The Goo Gel
FDA Label NDC 82503-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Apsm Performance, Llc for the product The Goo (NDC 82503-101). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients, purpose, uses, warnings, otc - keep out of reach of children, inactive ingredients, directions, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
TOPICAL PAIN RELIEF
Uses
Temporary relief of minor aches and pains of muscles and joints associated with arthritis, backache, strain, sprains, and bruises.
Warnings
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
KEEP OUT OF REACH OF CHILDREN.
Inactive Ingredients
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
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.
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