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Zeasorb jock itch - Medication Information

Product NDC Code 0316-8001
Drug Name

Zeasorb jock itch

Type Brand
Pharm Class Azole Antifungal [EPC],
Azoles [CS]
Active Ingredients
Miconazole nitrate 20 mg/g
Route TOPICAL
Dosage Form POWDER
RxCUI drug identifier 998461,
1437793
Application Number M005
Labeler Name Crown Laboratories
Packages
Package NDC Code Description
0316-8001-02 71 g in 1 bottle, plastic (0316-8001-02)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Miconazole nitrate 2%

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. 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 Aloe Barbadensis Leaf Juice Powder, Bentonite, Fragrance, Potassium Sorbate, Sodium Benzoate, Tapioca Starch, Tricalcium Phosphate, Water, 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 Proven clinically effective in the treament of most jock itch

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.
Zeasorb Jock Itch MICONAZOLE NITRATE ALOE VERA LEAF POTASSIUM SORBATE MICONAZOLE NITRATE MICONAZOLE SODIUM BENZOATE STARCH, TAPIOCA TRICALCIUM PHOSPHATE WATER STARCH, CORN BENTONITE

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 New & Improved Zeasorb®AF Antifungal Powder with 2% Miconazole Nitrate Cures Most Jock Itch Relieves Itching, Burning, Scaling Patented Odor Control Technology Attacks and Absorbs Moisture Talc-Free, Paraben-Free, Aluminum-Free Dermatologist Recommended Net wt. 2.5 oz (71g) P12322.00 Zeasorb JI

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. If irritation occurs or if there is no improvement within 2 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 help or contact a poison control center right away.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions? call 1-833-279-6522

Storage and handling

Information about safe storage and handling of the drug product.
Other information store at 20 o - 25 o C (68 o - 77 o F) [see USP Controlled Room Temperature]. Product settles during shipment. Package contains full net weight.

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