Label: BEILLOSO BALANITIS RELIEF- miconazole nitrate 2% balanitis relief cream

  • NDC Code(s): 85248-138-01
  • Packager: Jiangxi Yudexi Pharmaceutical Co., LTD
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 14, 2026

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  • Active Ingredient

    Miconazole Nitrate 2%

  • Purpose

    reduce inflammation.soothe irritated skin

  • Use

    Helps relieve redness, itching & irritation from balanitis,and soothes discomfort from other fungal skin conditions in sensitive areas.

  • Warnings

    For external use only.

  • Do not use

    under 2 years of age unless directed by a doctor.

  • When Using

    avoid contact with the eyes.If contact occurs. rinse the eyes very thoroughly with water

  • Stop Use

    if irritation occurs,symptoms perist for more than 2 weeks,or symptoms worsen after initial improvement.

  • Ask Doctor

    if irritation occurs,symptoms perist for more than 2 weeks,or symptoms worsen after initial improvement.

  • Keep Oot Of Reach Of Children

    lf swallowed. get medical help or contact a Poison Control Center right away.

  • Directions

    ·Dispense 2 pumps of cream onto clean fingers.·Apply to affected area on clean, dry skin 1-2x daily,gently massage until fully absorbed.·For first-time users: Do a small patch test before full use

  • Other information

    Store at 59-86°F(15-30°C）

  • Inactive ingredients

    water,allantoin.beeswax,cedarwood oil, cottonseed oil, jojoba oil lavender oil, magnesium oxide,MCT oil, silver stearate, zinc oxide.


  • PRINCIPAL DISPLAY PANEL

    2

  • INGREDIENTS AND APPEARANCE
    BEILLOSO BALANITIS RELIEF 
    miconazole nitrate 2% balanitis relief cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:85248-138
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE2 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALLANTOIN (UNII: 344S277G0Z)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    WATER (UNII: 059QF0KO0R)  
    JOJOBA OIL (UNII: 724GKU717M)  
    CEDRUS ATLANTICA BARK OIL (UNII: ZX5QRE4U60)  
    ZINC OXIDE (UNII: SOI2LOH54Z)  
    MAGNESIUM OXIDE (UNII: 3A3U0GI71G)  
    SILVER STEARATE (UNII: 4H6PCL92ZN)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    COTTONSEED OIL (UNII: H3E878020N)  
    BEESWAX (UNII: 2ZA36H0S2V)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:85248-138-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product02/10/2026
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00502/10/2026
    Labeler - Jiangxi Yudexi Pharmaceutical Co., LTD (455662836)
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