Label: AUQUEST NAIL REPAIRESSENCE- nail repairessence liquid

  • NDC Code(s): 84186-011-01
  • Packager: Guangzhou Bonnieco Cosmetics Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 2, 2024

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

View All Sections
  • Active Ingredient

    Salicy Acid 1.5%

  • Purpose

    skinconditioner, Antifungal

  • Use

    For the care of crackedand rough nails, nail
    discolorations, nail separation

  • Warnings

    For external useonly. Keep out of reach ofchildren

  • Do not use

    Discontinue use if signs ofirritation or rash occur andseek the assistance of adermatologist.

  • When Using

    In case of contact with the eyes, rinse immediately with plenty of water.

  • Stop Use

    If discomfort arises, please immediately stop using the product and seek the assistance of a dermatologist.

  • Ask Doctor

    If discomfort arises, please immediately stop using the product and seek the assistance of a dermatologist.

  • Keep Oot Of Reach Of Children

    Keep out of reach of children. If swallowed call emergency services.

  • Directions

    1. Soften nails with warm water.2.Use a manicure knife to
    2.repair the grooves on the nailsurface and remove dirt.
    3.Apply 3-4 drops of the nailessence to the infected nails.4.Twice a day in the morningand in the evening respectively.After every 2-3 days of use,polish the surface of the nailsand then continue to use..

  • Other information

    Store in a cool and dry place

  • Inactive ingredients

    WATER, HYDROGENATED CASTOR OIL, ACETIC ACID, PROPOLIS WAX, JEWELWEED EXTRACT, STEMONA JAPONICA EXTRACT, ANGELICA SINENSIS EXTRACT, CIMICIFUGA DAHURICA EXTRACT, PSEUDOLARIX AMABILIS ROOT BARK EXTRACT, ARTEMISIA ARGYI LEAF EXTRACT

  • PRINCIPAL DISPLAY PANEL

    12

  • INGREDIENTS AND APPEARANCE
    AUQUEST NAIL REPAIRESSENCE 
    nail repairessence liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84186-011
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ACETIC ACID (UNII: Q40Q9N063P)  
    PROPOLIS WAX (UNII: 6Y8XYV2NOF)  
    IMPATIENS CAPENSIS LEAF (UNII: QRM07CT8WJ)  
    STEMONA JAPONICA ROOT (UNII: FXG254HF10)  
    ANGELICA SINENSIS ROOT (UNII: B66F4574UG)  
    HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)  
    ARTEMISIA ARGYI LEAF (UNII: 2JYC99Q0WZ)  
    PSEUDOLARIX AMABILIS WHOLE (UNII: G2TMJ38TAU)  
    ACTAEA DAHURICA WHOLE (UNII: 790B636N1U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84186-011-0120 mL in 1 BOTTLE; Type 0: Not a Combination Product04/02/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00504/02/2024
    Labeler - Guangzhou Bonnieco Cosmetics Co., Ltd (412244189)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangzhou Bonnieco Cosmetics Co., Ltd412244189manufacture(84186-011) , label(84186-011)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!