Label: NAIL TREATMENT LIQUID (salicylic acid, chlorhexidine di- acetate liquid

  • NDC Code(s): 84336-002-01
  • Packager: Shenzhen Shenyuanye Trading Co., LTD
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 11, 2024

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

  • ACTIVE INGREDIENT

    SALICYLIC ACID 2%

    Chlorhexidine di(acetate) 2%

  • PURPOSE

    REMOVES FUNGUS

  • INDICATIONS & USAGE

    Uses For all caused by nail fungus

    nail discoloration

    nail thickening

    nail splitting

    nail crumbling

  • WARNINGS

    For external use on nailfungus(onychomycosis) only, pleasedon't use it on healthy nails.

  • DO NOT USE

    Don't use it on damafed skin,otherwise, your damaged skin maybe painful.

  • WHEN USING

    Don't drink, avoid contact with your eye.

  • STOP USE

    For people with severe skin ulceration, please use it with caution.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

    Children use it under thesupervision of adults.

  • ASK DOCTOR

    Stop use and ask a doctor if

    You are allergic to vinegar(such as itching, rash sweling ofthe lips, eyelids, and shortnessof breath)

  • DOSAGE & ADMINISTRATION

    Direction
    Apply it in the day and night(twice a day).
    Before using it for the first time,soak the diseased nail with warm water to soften it, use thenail file to polish the nail, make itthin cisibly, and scrape off thedirt on the nail (be careful not tohurt the nail hed), then apply theliquid.
    After first use, every 2-3 daysuse the nail file to polish thesur face of the diseased nail and then continue to use it.
    If seallowed, get medical help or contact a poison controlcenter right away.

  • INACTIVE INGREDIENT

    Water, Sorbitol, Alcohol, Propylene-Glycol, Angelica Dahurica,Laurocapram, Caramel, Dimethylol.Urea, Sunset Yellow.

  • QUESTIONS

    For the quesiton, please contact us bybaizelu@outlook.com

  • PRINCIPAL DISPLAY PANEL

    labeling

  • INGREDIENTS AND APPEARANCE
    NAIL TREATMENT LIQUID 
    salicylic acid, chlorhexidine di(acetate) liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84336-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLORHEXIDINE ACETATE (UNII: 5908ZUF22Y) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE2 mg  in 100 mL
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    SORBITOL (UNII: 506T60A25R)  
    LAUROCAPRAM (UNII: 1F3X9DRV9X)  
    CARAMEL (UNII: T9D99G2B1R)  
    WATER (UNII: 059QF0KO0R)  
    OXYMETHUREA (UNII: N68H97CAWG)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84336-002-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product06/11/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00506/11/2024
    Labeler - Shenzhen Shenyuanye Trading Co., LTD (550376513)
    Registrant - Shenzhen Shenyuanye Trading Co., LTD (550376513)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangzhou Mizi Biotechnology Co., Ltd.418001649manufacture(84336-002)