Label: FIFTHPULSE MICONAZOLE NITRATE ANTIFUNGAL- miconazole nitrate ointment

  • NDC Code(s): 87525-004-01, 87525-004-02
  • Packager: WeCare Products LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 2, 2026

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  • Drug Facts

  • Active ingredients

    Miconazole Nitrate 2%

    Purpose

    Anti-Fungal

  • Uses

    • Proven clinically effective in the treatment of most athlete's foot (tinea pedis) , jock itch (tinea cruris), and ringworm (tinea corporis)
    • Relieves itching, scaling, cracking, burning and discomfort associated with these conditions.
  • Warnings

    For external use only.

    Do not use 

    if the safety-sealed tube is punctured or damaged.

    Do not useon children 2 years of age unless directed by a doctor.

    When using this product

    avoid contact with eyes.

    Stop use and ask a doctor if

    • Irritation occurs or if there is no improvement within 4 weeks (for athlete's foot or ringworm) or within 2 weeks (for jock itch).
    • Irritation occurs, or if there is no improvement 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

    • 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 athelete's foot:Pay special attention to the spaces between the toes; • Wear well-fitting ventilated shoes • Change socks at least once daily.
    For ringworm:Use daily for 4 weeks. If condition persists, consult a doctor.
    For jock itch:Use daily for 2 weeks. If condition persists longer, consult a doctor. • This product is not effective on the scalp or nails.

  • Other information:

    • Store at 15° to 30° C (59° to 86°F) • Lot number and expiration date see crimp of tube or see box. • To open: Unscrew cap, tear safety seal off.

  • Inactive ingredients

    Alcohol, Carbomer, Cetostearyl alcohol, Dimethyl sulfoxide, Edetate disodium, Ethylparaben, Glycerol, Mineral oil, Mono-and-di-glycerides, Petrolatum, Polyoxyethylene lauryl ether, Purified water, Stearic acid, Triethanolamine.

  • Questions or Comments?

    Please call 1-888-209-5201

  • Package Labeling:

    Outer Package7Inner Package7

  • Package Labeling:

    Outer Package8Inner Package8

  • INGREDIENTS AND APPEARANCE
    FIFTHPULSE MICONAZOLE NITRATE ANTIFUNGAL 
    miconazole nitrate ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:87525-004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE20 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    DIMETHYL SULFOXIDE (UNII: YOW8V9698H)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    ETHYLPARABEN (UNII: 14255EXE39)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    WATER (UNII: 059QF0KO0R)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:87525-004-011 in 1 BOX04/30/2026
    128.4 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:87525-004-021 in 1 BOX04/30/2026
    2113.4 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00504/30/2026
    Labeler - WeCare Products LLC (085508446)
    Registrant - WeCare Products LLC (085508446)
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