Clotrimazole
- Dosage form
- SOLUTION
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Label updated
- 2026-06-03
- Retrieved
- 2026-09-07
- Active ingredients
- CLOTRIMAZOLE
Label information
Drug Facts
Active ingredient
Clotrimazole USP, 1%
Purpose
Antifungal
Uses
- cures most athlete's foot (tinea pedis), jock itch (tinea cruris), and ringworm (tinea corporis)
- effectively relieves
- itching
- cracking
- burning
- discomfort
which can accompany these conditions
Warnings
For external use only
Label information
Ask a doctor before use
- on children under 2 years of age
Label information
When using this product
- avoid contact with eyes
Label information
Stop use and ask a doctor if
- irritation occurs
- there is no improvement within 4 weeks (for athlete's foot and ringworm) or 2 weeks (for jock itch)
Label information
Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- This product is not effective on the scalp or nails For best results, follow directions and continue treatment for length of time indicated. For athlete's foot and ringworm: use daily for 4 weeks. For jock itch: use daily for 2 weeks.
- 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; change shoes and socks at least once daily
Other information
- Store at 20° to 25°C (68° to 77°F)[see USP Controlled Room Temperature].
Inactive ingredient
polyethylene glycol 400
Questions?
Call 1-866-923-4914
Label information
Distributed by:
Taro Pharmaceuticals U.S.A., Inc.
Hawthorne, NY 10532
Clotrimazole Topical Solution USP 1%
Clotrimazole Topical Solution USP 1%
[Image in the official label — see DailyMed source]
Clotrimazole Topical Solution 1%
[Image in the official label — see DailyMed source]
DailyMed Set ID: 13a14d3c-bfce-42b5-8463-4ec69e94774e · Version 5
NDC: 51672-2037, 51672-2158