Cbdmedic Foot Pain Relief
FDA Label NDC 24909-739

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 Foot Pain Relief (NDC 24909-739). 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 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.

Active Ingredients And Purpose

Camphor 10%, Menthol 15% (External Analgesics)

Uses

Temporarily relieves minor aches and pains of muscles and joints in the feet, toes and ankles.

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 ointment 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, cottonseed oil, eucalyptus oil, hemp extract (THC free), jojoba oil, peppermint oil, sorbic acid, tea tree oil

Principal Display Panel

Active Pain (24909 739 New.)

Active Pain (24909 739 New.)

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