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Maximum strength medicated foot powder - Medication Information

Product NDC Code 49035-795
Drug Name

Maximum strength medicated foot powder

Type Brand
Active Ingredients
Menthol .1 g/g
Route TOPICAL
Dosage Form POWDER
RxCUI drug identifier 259579
Application Number part348
Labeler Name Walmart Stores Inc
Packages
Package NDC Code Description
49035-795-01 283 g in 1 bottle, plastic (49035-795-01)
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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 adults and children 2 years of age and over: apply freely up to 3 or 4 times daily children under 2 years: consult a physician For best results, dry skin thoroughly before use.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
​Inactive ingredients benzethonium chloride, eucalyptus oil, peppermint oil, sodium bicarbonate, tricalcium phosphate, Zea mays (corn) starch

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.
​Use for the temporary relief of pain and itching associated with -minor cuts -scrapes -sunburn -insect bites -prickly heat -rashes -minor burns -minor skin irritation -dries the oozing of poison ivy, oak and sumac.

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 Medicated Foot Powder BENZETHONIUM CHLORIDE EUCALYPTUS OIL TRICALCIUM PHOSPHATE PEPPERMINT OIL SODIUM BICARBONATE ZEA MAYS WHOLE 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.
Maximum Strength Medicated Foot Powder label

Ask doctor

Information about when a doctor should be consulted about existing conditions or sumptoms before using the drug product, including all warnings for persons with certain preexisting conditions (excluding pregnancy) and all warnings for persons experiencing certain symptoms. The warnings under this heading are those intended only for situations in which consumers should not use the product until a doctor is consulted.
Stop and consult a doctor if conditions worsens redness, irritation, swelling or pain persist or increases symptoms do not get better within 7 days or clear up and occur again within a few days

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 (1-800-222-1222) right away.

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
​When using this product avoid contact with eyes. Not for genital area

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. ​When using this product avoid contact with eyes. Not for genital area Stop and consult a doctor if conditions worsens redness, irritation, swelling or pain persist or increases symptoms do not get better within 7 days or clear up and occur again within a few days ​Keep out of reach of children. In case of accidental ingestion, get medical help or contact a Poison Control Center (1-800-222-1222) 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