Active Ingredient And Purpose
Menthol 4% (External Analgesic)
Cbdmedic Arthritis Pain Relief
FDA Label NDC 24909-740
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Aidance Skincare & Topical Solutions, Llc for the product Cbdmedic Arthritis Pain Relief (NDC 24909-740). 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 ingredient and purpose, uses, warnings, keep out of reach of children, directions, inactive ingredients, principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Uses
Temporarily relieves minor aches and pains of muscles and joints associated with arthritis.
Warnings
For external use only. Do not use on wounds or damaged skin. When using this product: • avoid contact with eyes or mucous membranes • do not bandage tightly or use with a heating pad. Stop use and ask a doctor if: • condition worsens, or symptoms persist for more than 7 days • symptoms clear up and occur again within a few days • excessive skin irritation develops.
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a poison control center immediately.
Directions
Adults and children 12 years of age and older: massage cream into affected area not more than 3 to 4 times daily. Wash hands with soap and water after use. Children under 12 years of age: ask a doctor.
Inactive Ingredients
Beeswax (organic), clove oil, cotton seed oil, emulsifying wax, eucalyptus oil, hemp extract (THC-free), jojoba seed oil, peppermint oil, purified water, shea butter, sorbic acid, tea tree oil
Principal Display Panel
Image Description (24909 728 New)
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