FDA Label for Cbd Unlimited Topical Analgesic
View Indications, Usage & Precautions
Cbd Unlimited Topical Analgesic Product Label
The following document was submitted to the FDA by the labeler of this product Endexx Corporation. 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 USP 5%
Camphor 3.25%
Purpose
Topical Analgesic
Uses
Temporary relief from minor aches and pains of muscles & joints associated with: arthritis, simple backache, strains, sprains
Warnings:
For external use only.
When using this product:
• use only as directed
• do not bandage tightly or use with a heating pad
• avoid contact with eyes and mucous membranes
• do not apply to wounds or damaged, broken or irritated skin
• do not spray onto face
• avoid inhaling spray mist and fumes
Stop use and ask doctor if:
• condition worsens
• redness is present
• irritation develops
• symptoms persist for more than 7 days or clears up and occurs again within a few days
Flammable
do not use near heat or open flame or while smoking
If pregnant or breast-feeding, ask a healthcare professional before use
Keep Out Of Reach Of Children
If product is swallowed get medical help or contact a Poison Control Center right away.
Directions:
FOR EXTERNAL USE ONLY:
Shake Before Using
Adults and children 12 years of age and older:
Spray on affected areas 1 to 4 times daily.
Avoid contact with eyes and mouth.
Inactive Ingredients
Arnica Extract (Glycerin, Water, Arnica Montana Flower Extract), Clove Bud Oil, Eucalyptus Globulus Leaf Oil, Hemp-Derived Cannabidiol Isolate, Isopropyl Alcohol, Methylsulfonylmethane (MSM), Wintergreen Oil (Methyl Salicylate)
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