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| Product NDC Code | 41167-0171 | ||||||
|---|---|---|---|---|---|---|---|
| Drug Name | Gold bond medicated maximum strength foot |
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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 | Chattem, 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 i ngredient Menthol 1%
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 and older: apply freely up to 3 or 4 times daily ■ children under 2 years: ask a doctor ■ thoroughly wash and dry feet, sprinkle powder liberally over feet, between toes and on bottoms of feet. Sprinkle inside shoes for maximum freshness.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.In active ingredients zea mays (corn) starch, sodium bicarbonate, acacia senegal gum, silica, tricalcium phosphate, eucalyptus globulus leaf oil, mentha piperita (peppermint) oil, benzethonium chloride
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 s temporarily relieves the pain and itch associated with: ■ minor skin irritations on the foot
Purpose
Information about the drug product’s indications for use.Purpose Anti-itch
Spl product data elements
Usually a list of ingredients in a drug product.Gold Bond Medicated Maximum Strength Foot Menthol MENTHOL MENTHOL STARCH, CORN SODIUM BICARBONATE ACACIA SILICON DIOXIDE TRICALCIUM PHOSPHATE EUCALYPTUS OIL PEPPERMINT OIL BENZETHONIUM CHLORIDE
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 GOLD BOND MEDICATED MAXIMUM STRENGTH FOOT POWDER ANTI-ITCH MENTHOL 1% TRIPLE ACTION FORMULA Net Wt 10 oz (283 g) GOLD BOND MEDICATED MAXIMUM STRENGTH FOOT POWDER ANTI-ITCH MENTHOL 1% TRIPLE ACTION FORMULA Net Wt 10 oz (283 g)
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.Gold Bond Medicated Foot Powder Drug Facts
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. If swallowed, get medical help or contact a Poison Control Center immediately.
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 a few days ■ redness, irritation, swelling or pain persists or increases
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
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 Stop use and ask a doctor if ■ condition worsens ■ symptoms persist for more than 7 days or clear up and occur again within a few days ■ redness, irritation, swelling or pain persists or increases 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