Label: CLOTRIMAZOLE solution

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 18, 2024

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  • Active ingredient

    Clotrimazole USP, 1%

  • Purpose

    Antifungal

  • Uses

    Cures most

    • Athlete’s foot (tinea pedis),
    • Jock itch (tinea cruris), and
    • Ringworm (tinea corporis).

    Effective relieves

    • itching

    • cracking

    • burning

    • discomfort which can accompany these conditions

  • Warning

    For external use only

  • Ask a doctor before use

    • on children under 2 years of age
  • When using this product

    avoid contact with eyes

  • 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)
  • Keep out of the 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 between 15°-30°C (59°-86°F)

  • Inactive ingredient

    polyethylene glycol

  • Questions or comments?

    Call 1-877-770-3183 Mon-Fri 9:00 AM to 4:30 PM EST

  • Clotrimazole 1% Topical Solution

    10 mL

  • INGREDIENTS AND APPEARANCE
    CLOTRIMAZOLE 
    clotrimazole solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0536-1181
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CLOTRIMAZOLE (UNII: G07GZ97H65) (CLOTRIMAZOLE - UNII:G07GZ97H65) CLOTRIMAZOLE1 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0536-1181-7010 mL in 1 BOTTLE; Type 0: Not a Combination Product08/20/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00508/20/2018
    Labeler - RUGBY LABORATORIES (079246066)
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