FDA Label for Blue Goo Pain Relieving
View Indications, Usage & Precautions
Blue Goo Pain Relieving Product Label
The following document was submitted to the FDA by the labeler of this product Garcoa, Inc.. 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 Ingredient
Menthol 2.5%
Purpose
- Topical Analgesic
Uses
For the temporary relief of muscle aches, pains and strains, arthritic pain, joint pain, and tendonitis
Warnings
For external use only
• Avoid contact with eyes •Do not apply to wounds or damaged skin • Do not bandage tightly •Do not use with heating pads or heating devices •Discontinue use and consult a doctor if condition worsens or if symptoms persist for 7 days or more or clear up and occur again within a few days, or if pain, swelling or redness occurs after continued use
Directions
Directions
Adults and children 6 years of age and older apply liberally to affected area not more than 3-4 times daily. Children under 6 years of age: Do Not Use.
Inactive Ingredients
water, dimethyl sulfone, emu oil, alcohol denat., sodium chondroitin sulfate, glucosamine HCl, camphor, chrysanthemum parthenium (Feverfew) extract, arnica montana flower extract, chamomilla recutita (Matricaria) flower extract, urtica dioica (Nettle) extract, hamamelis virginiana (Witch Hazel) extract, calendula officinalis extract, salix alba (Willow) bark extract, coriandrum sativum (Coriander) extract, aloe barbadensis leaf juice, eucalyptus globulus leaf oil, fragrance, sodium hydroxide, carbomer, sorbitol, methyl salicylate, phenoxyethanol, blue 1
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Blue Goo Pain
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