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Touchless Care ANTIFUNGAL

Dosage form
SPRAY
Labeler
Crawford Healthcare, Inc.
Label updated
2017-02-16
Retrieved
2026-09-07
Active ingredients
MICONAZOLE NITRATE
View original label and images on DailyMed ↗
Active Ingredient

Miconazole Nitrate 2%

Purpose

Antifungal

Indications
  • Treats jock itch, ringworm and athlete's foot
  • For the treatment of most superficial skin irritations caused by yeast (Candida albicans). Follow a physician's instructions when treating Candida.
Warnings

Do not use on children under 2 years of age unless directed by a doctor. Not intended for ingestion. Do not use for diaper rash. For external use only. When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if
  • irritation develops
  • there is no improvement within 4 weeks for athlete's foot or ringworm or within 2 weeks for jock itch.
Keep out of reach of children.

If swallowed, get medical help or contact a poison control center immediately.

Directions
  • Cleanse the affected area and allow to dry.
  • Shake bottle well before use.
  • Spray 4-6 inches from skin twice daily (morning and night) or as directed by a physician. No rub-in is required.
  • For athlete's foot and ringworm, use daily for 4 weeks. For jock itch, use daily for 2 weeks. If condition persists longer, contact a doctor. This product is not effective on the scalp or nails.
Other Information

Store at 59 oF - 87 oF (15 oC - 30 oC)

Inactive Ingredients

Cyclomethicone, Dimethicone, Hexamethyldisiloxane, Lanolin, Light Mineral Oil, Microcrystalline Wax, Vitamin A Palmitate, Vitamin D3, White Petrolatum, Zinc Oxide

SPL Unclassified Section

Distributed by: Crawford Healthcare, Inc. Doylestown, PA 18901

Touchless Care is a registered trademark of Crawford Woundcare Ltd.

© Crawford Healthcare Ltd., 2016

www.crawfordhealthcare.com/us

1-855-522-2211

Made in the USA

Package Label

Antifungal label

[Image in the official label — see DailyMed source]

DailyMed Set ID: 48a7a01e-3480-45bf-e054-00144ff88e88 · Version 1
NDC: 69502-001