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Mycozyl AP

Dosage form
POWDER
Labeler
PureTek Corporation
Label updated
2024-10-01
Retrieved
2026-09-07
Active ingredients
MICONAZOLE NITRATE
View original label and images on DailyMed ↗
Active ingredient

Miconazole Nitrate 2.0%

Purpose

Antifungal

Uses
  • for the treatment of most athlete's foot (tinea pedis), jock itch (tinea cruris), ringworm (tinea corporis)
  • relieves itching, scaling, cracking, burning, redness, soreness, irritation, discomfort and chafing associated with jock itch
주의사항

For external use only.

Do not use on

■ children under 2 years of age unless directed by a doctor

When using this product

  • do not get into eyes

Stop use and ask a doctor if

  • for athlete's foot and ringworm - irritation occurs or there is no improvement within 4 weeks
  • for jock itch - irritation occurs or there is no improvement within 2 weeks

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

■ clean 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.

Other information

■ protect from freezing ■ avoid excessive heat ■ do not use if package is damaged

Inactive ingredients

Aleurites Moluccana (Kukui) Seed Oil, Aloe Barbadensis (Aloe Vera) Leaf Juice Powder, Bisabolol, Carthamus Tinctorius (Safflower) Oleosomes, Fragrance, Nylon-12, Silica, Sodium Benzoate, Sodium Hyaluronate, Zea Mays (Corn) Starch, Zingiber Officinale (Ginger) Root Extract.

Mycozyl Antifungal Powder

[Image in the official label — see DailyMed source]

DailyMed Set ID: b3c46a30-7ff2-0dc4-e053-2995a90aa571 · Version 5
NDC: 59088-442