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| Product NDC Code | 73096-746 | ||||||||
|---|---|---|---|---|---|---|---|---|---|
| Drug Name | Cbdmedic foot and ankle pain relief |
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| Type | Brand | ||||||||
| Active Ingredients |
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| Route | TOPICAL | ||||||||
| Dosage Form | OINTMENT | ||||||||
| Application Number | part348 | ||||||||
| Labeler Name | ABACUS HEALTH PRODUCTS, INC. | ||||||||
| Packages |
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| Check if available Online | Get Medication Prices online with Discount |
Active ingredient
A list of the active, medicinal ingredients in the drug product.Active Ingredients and Purpose Camphor 10%, Menthol 15% (External Analgesics)
Dosage and administration
Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.Directions Adults and children 12 years of age and older: • apply to affected area not more than 3 to 4 times daily Children under 12 years of age: ask a doctor
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive ingredients Cottonseed oil, beeswax, CBD hemp oil, clove oil, eucalyptus oil, jojoba seed oil, peppermint oil, tea tree oil, sorbic acid
Indications and usage
A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.Uses Temporary relief of minor aches and pains of muscles and joints associated with feet, toes and ankles
Spl product data elements
Usually a list of ingredients in a drug product.CBDMEDIC Foot and Ankle Pain Relief Camphor and Menthol WHITE WAX CLOVE OIL COTTONSEED OIL EUCALYPTUS OIL HEMP JOJOBA OIL PEPPERMINT OIL SORBIC ACID TEA TREE OIL CAMPHOR (NATURAL) CAMPHOR (NATURAL) MENTHOL MENTHOL
Package label principal display panel
The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.PRINCIPAL DISPLAY PANEL Label
Spl unclassified section
Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.Questions? Call 1-844-422-3633
Warnings
Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.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 • symptoms persist for more than 7 days • symptoms clear up and occur again within a few days • excessive skin irritation develops If pregnant or breast-feeding ask a health professional before use Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center immediately
Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API