Label: ANTIFUNGAL- clotrimazole cream

  • NDC Code(s): 67777-727-01, 67777-727-02, 67777-727-03, 67777-727-04, view more
    67777-727-05
  • Packager: Dynarex Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 18, 2026

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  • Active ingredient

    Clotrimazole USP 1%

  • Purpose

    Antifungal

  • Uses

    • For the treatment of most athlete's foot (tinea pedis), jock itch (tinea cruris), and ringworm (tinea corporis)

    • Relieves itching, scaling, burning, redness, soreness, irritation, discomfort, and chafing associated with jock itch and itching, burning feet

  • Warnings

    • Do not use on children under 2 years of age unless directed by a doctor

    • For external use only

    • Avoid contact with eyes

    Stop use and ask a doctor if

    • Irritation occurs or if there is no improvement within 4 weeks, discontinue use and consult a doctor for athlete's foot and ringworm.

    • Irritation occurs or if there is no improvement within 2 weeks, discontinue use and consult a doctor for jock itch.

    Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away

  • Directions

    • Clean the affected area and dry thoroughly. Apply a thin layer 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. • If condition persists longer, consult a doctor. • This product is not effective on the scalp or nails.

  • Other information

    • Store at controlled room temperature 20°-25°C (68°-77°F)

    • Tamper evident. Do not use if seal is damaged.

  • Inactive ingredients

    ceteth-20, cetostearyl alcohol, light mineral oil, methylparaben, propylene glycol, propylparaben, purified water, petrolatum

  • Label 1231-C

    1231-C_IN_MASTER

  • Label 1233-C

    1233-C_IN_MASTER

  • INGREDIENTS AND APPEARANCE
    ANTIFUNGAL 
    clotrimazole cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-727
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CLOTRIMAZOLE (UNII: G07GZ97H65) (CLOTRIMAZOLE - UNII:G07GZ97H65) CLOTRIMAZOLE1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    LIGHT MINERAL OIL (UNII: N6K5787QVP)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    CETETH-20 (UNII: I835H2IHHX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67777-727-0272 in 1 CASE03/24/2026
    1NDC:67777-727-0128.4 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:67777-727-054 in 1 CASE03/24/2026
    2NDC:67777-727-046 in 1 BOX
    2NDC:67777-727-03113 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00503/24/2026
    Labeler - Dynarex Corporation (008124539)
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