Label: ANTIFUNGAL CREAM cream

  • NDC Code(s): 84048-004-01
  • Packager: Shenzhen Peruidaishi Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 25, 2024

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  • Active Ingredient

    Miconazole nitrate 2%

  • Purpose

    Recuren Plus AntifungalCream, is equipped withreparative and anti-itchcapabilities.

  • Use

    The product with Repairand Anti-ltch functioneffectively relieve skindiscomfort, such asitching, athlete's footeczema, jock itch, etc.

  • Warnings

    For external use only.Avoid direct contactwith eyes.If irritation occurs,discontinue use.Keep out of reach ofchildren.Store in a cool, darkplace.

  • When Using

    1. First test a smallpatch of skin to checkfor any potentialallergic reaction.

    2. Apply topically 2-3times daily to theaffected area.

  • Stop Use

    Stop use if there is no improvement within 4 weeks.

  • Keep Oot Of Reach Of Children

    Keep Oot Of Reach Of Children

  • Directions

    1. First test a smallpatch of skin to checkfor any potentialallergic reaction.

    2. Apply topically 2-3times daily to the affected area.

  • Other information

    Keep it away from children. Seal the bottle and place it in a cool and dry place.

  • Inactive ingredients

    Stemona
    Euphorbia
    Dictamnus
    Sophora Flavescens
    Aloe
    Cnidium
    Chlorhexidine acetate
    Vitamin E
    Borneol
    Natural menthol
    Stearic acid
    Medical vaseline
    Light liquid paraffin
    Glycerin
    Triethanolamine
    Purified water

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    ANTIFUNGAL CREAM 
    antifungal cream cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84048-004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    EUPHORBIA NERIIFOLIA LEAF (UNII: IRZ1UXK5K9)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    VASICINONE (UNII: G6T5819NXM)  
    LIGHT MINERAL OIL (UNII: N6K5787QVP)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)  
    CHLORHEXIDINE ACETATE (UNII: 5908ZUF22Y)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    STEMONA JAPONICA ROOT (UNII: FXG254HF10)  
    DICTAMNUS DASYCARPUS ROOT (UNII: 6153LEN214)  
    ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)  
    BORNEOL (UNII: M89NIB437X)  
    ALOE (UNII: V5VD430YW9)  
    MENTHOL (UNII: L7T10EIP3A)  
    WATER (UNII: 059QF0KO0R)  
    CNIDIUM MONNIERI FRUIT (UNII: V1IA3S3CUS)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84048-004-0160 g in 1 BOTTLE; Type 0: Not a Combination Product01/24/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00501/24/2024
    Labeler - Shenzhen Peruidaishi Technology Co., Ltd. (706728459)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Peruidaishi Technology Co., Ltd.706728459manufacture(84048-004) , label(84048-004)
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