Official product label reference

Jock Itch Powder — Premier Brands of America Inc

This page contains 13 source sections for MICONAZOLE NITRATE, topical route. Label set 5aaacc88-6752-ab47-e063-6394a90af7cd, version 1.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

Uses for the cure of most athlete's foot, jock itch and ringworm

Purpose

Purpose Antifungal

Dosage and administration — label text

Directions clean the affected area and dry thoroughly apply a thin layer of 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 conditions persist longer, consult a doctor this product is not effective on the scalp or nails

Warnings

Warnings For external use only. Do not use on children under 2 years of age unless directed by a doctor. When using this product avoid contact with the eyes Stop use and ask a doctor if irritation occurs or there is no improvement within 4 weeks for athlete's foot and ringworm, or 2 weeks for jock itch. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Active ingredient

Active ingredient Miconazole nitrate 2%

Do not use

Do not use on children under 2 years of age unless directed by a doctor.

While using this medicine

When using this product avoid contact with the eyes

When to stop use and seek help

Stop use and ask a doctor if irritation occurs or there is no improvement within 4 weeks for athlete's foot and ringworm, or 2 weeks for jock itch.

Child safety

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Other safety information

Other information store between 59º - 86ºF lightly shake bottle to loosen settled powder

Inactive ingredient

Inactive ingredients zea mays (corn) starch, tricalcium phosphate, microcrystalline cellulose, sodium bicarbonate, allantoin, chloroxylenol, fragrance

Questions

Questions? Call 1-866-964-0939

Recent major changes

Official sources and product identifiers

DailyMed — complete source labelVerify the current version and original formatting, including tables and diagrams.
openFDA — structured source recordMachine-readable label source, linked by the exact label set ID.

Substances listed: MICONAZOLE NITRATE

RxNorm identifiers: 998461

Package NDC codes

56104-122-01

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.

Jock Itch Powder drug information