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Lotrimin Af Jock Itch

Generic: Miconazole Nitrate

OTC
✓ FDA-verified
View full FDA label ↗
Lotrimin Af Jock Itch is a spray used to treat jock itch, which is a fungal infection that causes itching, burning, and discomfort in the groin area. It works by targeting the fungus responsible for the infection, helping to relieve symptoms. To use it, wash and dry the affected area, then shake the can well and spray a thin layer over the area twice a day, in the morning and at night, for up to two weeks. It's important to note that this medication should not be used on children under 2 years of age unless directed by a doctor. Additionally, avoid using it near heat or flames, as it is flammable.
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Uses

  • jock itch (tinea cruris).
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Dosage

Wash and dry the affected area thoroughly.
Shake the can well before use.
Spray a thin layer over the affected area twice daily (morning and night).
Use daily for 2 weeks.
If the condition persists longer, ask a doctor.
This product is not effective on the scalp or nails.
Always follow your doctor's specific instructions for your dose.
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Side effects

Common

Irritation at the application siteNo improvement within 2 weeks
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Warnings

⚠ Important warnings

  • For external use only.
  • Flammable: Do not use while smoking or near heat or flame.
  • Do not use on children under 2 years of age unless directed by a doctor.
  • Avoid contact with the eyes.
  • Use only as directed.
  • Intentional misuse can be harmful or fatal.
  • Contents under pressure; do not puncture or incinerate.
  • Do not store at temperatures above 120°F.
  • Keep out of reach of children.
  • If swallowed, get medical help or contact a Poison Control Center right away.

Ask about this product

Answers pulled from the FDA label only.

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Medical Disclaimer: This content is provided for informational and educational purposes only and is not intended as medical advice. Always consult a qualified healthcare provider before taking any medication.
Data Source: Publicly available drug labeling information from the U.S. Food and Drug Administration (FDA).