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Db antifungal foot - Medication Information

Product NDC Code 43689-0025
Drug Name

Db antifungal foot

Type Brand
Pharm Class Azole Antifungal [EPC],
Azoles [CS]
Active Ingredients
Miconazole nitrate 20 mg/g
Route TOPICAL
Dosage Form CREAM
RxCUI drug identifier 998483
Application Number M005
Labeler Name The Magni Group Inc
Packages
Package NDC Code Description
43689-0025-1 113 g in 1 jar (43689-0025-1)
43689-0025-2 1 jar in 1 box (43689-0025-2) / 113 g in 1 jar
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredients (in cream) Miconazole Nitrate 2% Purpose Antifungal

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 • Wash the affected area and dry thoroughly • Apply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor • Supervise children in the use of this product • For athlete’s foot: Pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily • For athlete’s foot and ringworm, use daily for 4 weeks; for jock itch, use daily for 2 weeks • If condition persists longer, consult a doctor • This product is not effective on the scalp or nails

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Allium Sativum Garlic (Plant) Extract, C12-15 Alkyl Benzoate, Ceteth-20, Cetyl Alcohol, Ethylhexylglycerin, Eucalyptus Globulus Leaf Oil, Garcinia Indica Seed Butter, Hydroxyacetophenone, Isopropyl Palmitate, Isopropyl Myristate, Lemon Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Phenoxyethanol, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Sodium Acrylate/Sodium Acryldimethyl Taurate Copolymer, Tocopheryl Acetate, Water

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 • Cures most tinea pedis (athlete’s foot) • Relieves itching, scaling, cracking, burning, redness; itchy, scaly skin between toes; itching, burning feet; discomfort

Purpose

Information about the drug product’s indications for use.
Purpose Antifungal

Spl product data elements

Usually a list of ingredients in a drug product.
DB Antifungal foot MICONAZOLE NITRATE ALKYL (C12-15) BENZOATE CETETH-20 CETYL ALCOHOL ETHYLHEXYLGLYCERIN EUCALYPTUS OIL GARCINIA INDICA SEED BUTTER ISOPROPYL PALMITATE ISOPROPYL MYRISTATE LEMON OIL TEA TREE OIL PHENOXYETHANOL ALMOND OIL .ALPHA.-TOCOPHEROL ACETATE WATER MICONAZOLE NITRATE MICONAZOLE

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.
Package Labeling: 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.
Drug Facts

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
Do not use on children under 2 years of age unless directed by a doctor • For external use only Avoid contact with the eyes If irritation occurs or if there is no improvement within 4 weeks, discontinue use and consult a doctor

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 attention, help, or contact a poison control center right away

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 Do not use on children under 2 years of age unless directed by a doctor • For external use only Avoid contact with the eyes If irritation occurs or if there is no improvement within 4 weeks, discontinue use and consult a doctor Keep out of reach of children • If swallowed, get medical attention, 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