Active Ingredients
Menthol 9.94%
Arnica Montana 4.97%
Methyl Salicylate 0.5%
Magneleaf Cbd Thc
FDA Label NDC 82900-112
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by M J Green Enterprises, Inc. for the product Magneleaf Cbd Thc (NDC 82900-112). 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, when using this product, stop use and consult a doctor if:, if pregnant of breast-feeding:, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Topical Analgesic
Uses
Temporary relief of aches and pains associated with, arthritis, carpal tunnel, swelling, sprains, bruising, inflammation
Warnings
For external use only
When Using This Product
Do not apply to wounds or irritated skin. Avoid contact with eyes, avoid use on deep wounds, avoid if you are allergic to listed ingredients.
Stop Use And Consult A Doctor If:
Condition worsens, Symptoms last for more than 7 days, condition clears up but occurs again in a few days, rash or irritation occurs.
If Pregnant Of Breast-Feeding:
Consult a health professional before use
Directions
Dosage: Apply to affected area 1 to 4 times daily, or as needed.
Keep Out Of Reach Of Children
Keep Out of Reach of Children
Other Information
Store at 66-92 Degrees Fahrenheit.
Avoid direct sunlight.
Inactive Ingredients
Shea Butter, Jojoba Oil, Beeswax, Coconut Oil, Water, Vitamin E Oil, Magnesium Chloride, Cannabidiol Oil, Tetrahydrocannabinol Acetate, Maranta Arundinacea Root Powder
6 Ounce Jar Label
MagneLeaf Pain Relief CBD THC Label
6 Ounce Lid Label
MagneLeaf THC Pain Relief Lid Label
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