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| Product NDC Code | 42669-283 | ||||
|---|---|---|---|---|---|
| Drug Name | Maximum strength medicated foot powder |
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| Type | Brand | ||||
| Active Ingredients |
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| Route | TOPICAL | ||||
| Dosage Form | POWDER | ||||
| RxCUI drug identifier | 259579 | ||||
| Application Number | M017 | ||||
| Labeler Name | Davion, Inc | ||||
| Packages |
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Active ingredient
A list of the active, medicinal ingredients in the drug product.Active Ingredient Menthol 1.0%
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 Remove seal beneath cap before first use. Do not use if seal is broken adults and children 2 years and older - apply freely upto 3 or 4 times daily children under 2 years - ask a doctor For best results, dry skin throughly before applying
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive ingredients Zea Mays (Corn) Starch, Tricalcium Phosphate, Sodium Bicarbonate, Benzethonium Chloride, Eucalyptus Oil, Peppermint Oil
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 pain and itch associated with: minor cuts sunburn insect bites scrapes minor burns minor skin irritations
Purpose
Information about the drug product’s indications for use.Purpose External Analgesic
Spl product data elements
Usually a list of ingredients in a drug product.Maximum Strength Medicated Foot Powder Menthol STARCH, CORN TRICALCIUM PHOSPHATE SODIUM BICARBONATE EUCALYPTUS OIL BENZETHONIUM CHLORIDE PEPPERMINT OIL 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 NDC 42669-283-01 CVS HEALTH Compared to the active ingredient in Maximum Strength Gold bond Medicated Foot Powder* MAXIMUM STRENGTH Medicated Foot Powder WITH CORNSTARCG Triple Relief: controls odor, absorbs moisture & relieves itc Soothing formula Clinically tested Talc free NET WT 10 OZ (283 g) Label
Keep out of reach of children
Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.Keep out of reach of children In case of accidental ingestion, get medical help or contact a poison control center right away.
Stop use
Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days or clear up and occur again within few days
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.Warning For external use only Avoid contact with eyes Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days or clear up and occur again within few days Keep out of reach of children In case of accidental ingestion, get medical help or contact a poison control center right away.
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