Label: CLEANING DISINFECTANT liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated April 28, 2020

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

  • DOSAGE & ADMINISTRATION

    Store itin a cool and dry place.

  • INACTIVE INGREDIENT

    water

  • INDICATIONS & USAGE

    Enviironmental suface:10 mins Spraying to wet.

    Object surface: 10 mins Soaking soubbing and spraying.

    Fabrics:10 mins Soaking

  • ACTIVE INGREDIENT

    BENZALKONIUM BROMIDE

    HEXAMETHYLENETETRAMINE

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of children

  • PURPOSE

    Disinfection
    Sterilization

  • WARNINGS

    1.Disinfectants for extermal use should not be taken orally, and keepit out of children's reach.
    2 Avoid contact with antagonists.
    3.Store itin a cool and dry place. If itis keptin a low temperature for a long time, itmay precipitate, but itwill not affect the quality of the product. Itcan be used onlywhen it is heated to room temperature.

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    CLEANING DISINFECTANT 
    cleaning disinfectant liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54796-003
    Route of AdministrationEXTRACORPOREAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    METHENAMINE (UNII: J50OIX95QV) (METHENAMINE - UNII:J50OIX95QV) METHENAMINE250 g  in 2500 g
    BENZALKONIUM BROMIDE (UNII: 151T1GQ42D) (BENZALKONIUM BROMIDE - UNII:151T1GQ42D) BENZALKONIUM BROMIDE125 g  in 2500 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code ecofinest
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54796-003-012500 g in 1 BOTTLE; Type 0: Not a Combination Product04/28/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other04/28/2020
    Labeler - Wuxi Youjie Technology Co. LTD (547669922)
    Establishment
    NameAddressID/FEIBusiness Operations
    Wuxi Youjie Technology Co. LTD547669922manufacture(54796-003)