Label: RECUREN PLUS FUNGAL NAIL RENEWAL- fungal nail renewal liquid

  • NDC Code(s): 84048-001-01
  • Packager: Shenzhen Peruidaishi Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 25, 2024

If you are a consumer or patient please visit this version.

  • Active Ingredient

    Miconazole nitrate 2%

  • Purpose

    Antifungal

  • Use

    This product facilitates the recovery of nailsinfluenced by nail fungus and aids in avertingrecurrent athlete's foor through daily usage.lteffectively targets diverse conditions likeomychomycosis, atrophy, uneven surfacesmstratification, nail thickening, yellowing, nailremoval, turbidity, discoloration, and other nailirregulartes.Beyondresoling these concerns,our product goes further by nurturing nails,encouraging their natural repair process, andgently reinstating theirinnate smoothness andluster.

  • Warnings

    * Do not use the product on children under 10 years ofage unless directed by a doctor.

    *Forexternal use only. if swallowed, seek immediatemedical assistance.

    *Safeguard the product from children to avert anychance of accidentalingestion..lmmediate discontinuation is advised in case of
    discomfort or irritation.

    * Refrain from applying the product on injured orswollen skin areas.

    *Forindividuals with sensitive skin, a patch test on thewrist's interior isrecommended before use,ensuring anirritation-free experience.

    *Keep the product away from the eyes to preventcontact.

  • Do not use

    Do not use the product on children under 10 years ofage unless directed by a doctor.
    lmmediate discontinuation is advised in case of discomfort or irritation.

  • When Using

    It is normal for nails to temporarilyexhibit a yellow hue during treatmentdue to the liquid's color.This willgradually recede as your toenailsregain their health.

  • Stop Use

    immediate discontinuation is advised in case of discomfort or irritation.

  • Keep Oot Of Reach Of Children

    Keep Out Of Reach Of Chlidren

  • Directions

    Begin by soaking your feetvom warm water for 5minutes. Afterward, ensure thorough drying of yourto es.
    Emnploy a fingemail clipper (not included) and a nailfile to meticulously eliminate as much damaged nailarea as possible.This pivotalstep maximizes theabsorption potential of our nail fungus treatment liquidApply an appropriate quantity of the liquid to theareas requiring repair.Repeat this proces 2-3 times daily until a healthy nailstarts its gradual regeneration, For optimal results,maintain usage for a continuous 6-week period.

  • Other information

    Store the productin a cool, shaded place, shieldedfrom direct sunight.Maintain atroom temperaturebetween 15-300c(59-86*). To prevent any accidents,keep it out of children's reach.

  • Inactive ingredients

    Water
    Sorbitol
    Alcohol
    Propylene Glycol
    Angelica Dahurica Root
    Laurocapram
    Caramel
    Dimethylol Urea
    FD&C Yellow No. 6

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    RECUREN PLUS FUNGAL NAIL RENEWAL 
    fungal nail renewal liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84048-001
    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
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    LAUROCAPRAM (UNII: 1F3X9DRV9X)  
    CARAMEL (UNII: T9D99G2B1R)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    OXYMETHUREA (UNII: N68H97CAWG)  
    SORBITOL (UNII: 506T60A25R)  
    ALCOHOL (UNII: 3K9958V90M)  
    ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84048-001-0130 mL 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(84048-001) , label(84048-001)