FDA Label for The Goo Medicated Pain Relief
View Indications, Usage & Precautions
The Goo Medicated Pain Relief Product Label
The following document was submitted to the FDA by the labeler of this product Apsm Performance, Llc. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredients
Methyl Salicylate 30%
Menthol 10%
Camphor 4%
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.
* Please review the disclaimer below.