Label: GERM AWAY- anti-microbial wipe cloth

  • NDC Code(s): 74680-101-63
  • Packager: Unico International Trading Corp
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 12, 2023

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

View All Sections
  • Active Ingredient

    Benzalkonium Chloride 0.1%

  • Keep out of the reach of children.

    Keep out of reach of children, except with adult supervision.

  • Warnings

    For external use only. Do not use in the eyes.

    Keep out of eyes. In case of eye contact, rinse with water. If irritation develops, discontinue use. Consult doctor if irritation persists for more than 72 hours.

    If swallowed, seek medical attention or contact a Poison Control Center.

  • Use

    For use: gently pull wipe from the dispenser feed at an angle and in a downward motion. wet hands or surface thoroughly with the product and let dry, discard wipe in trash

  • Inactive Ingredients

    Aqua, Decyl Glucoside, Glycerin, Sodium Hydroxymethylglycinate, Citric Acid, PEG-12 Dimethicone Copolyol, Tetrasodium EDTA, Potassium Sorbate, Sodium Benzoate, Aloe Barbadensis Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract, Allantoin, Panthenol, Tocopheryl Acetate

  • Purpose

    Anti-bacterial

  • To dispense

    Break tab on bucket rim and pull off cover. Open bag inside to expose wipes. Then thread center wipe through the lid. Replace bucket cover to maintain moisture.

  • To use

    Pull one sheet from pack. Sanitize hands or other affected area. Discard in trash after use. Do not flush. Close tab after use to retain moisture.

  • Package Label

    Germ Away 400

  • INGREDIENTS AND APPEARANCE
    GERM AWAY 
    anti-microbial wipe cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74680-101
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    SODIUM HYDROXYMETHYLGLYCINATE (UNII: DIG6BWZ9XT)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CHAMOMILE (UNII: FGL3685T2X)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    ALLANTOIN (UNII: 344S277G0Z)  
    2,2'-OXYDIPROPANOL (UNII: 7KOI7K0DHI)  
    COUMARIN (UNII: A4VZ22K1WT)  
    DIPHENYL ETHER (UNII: 3O695R5M1U)  
    3,7-DIMETHYL-1-OCTANOL (UNII: DPY9K1927C)  
    CP FORMATE (UNII: CEB8Q6WHK2)  
    TETRAHYDROLINALOOL (UNII: UM4XS5M134)  
    EUCALYPTOL (UNII: RV6J6604TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74680-101-63400 g in 1 CONTAINER; Type 0: Not a Combination Product05/28/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00305/28/2020
    Labeler - Unico International Trading Corp (805757200)
    Registrant - Dan Mor (514523067)
    Establishment
    NameAddressID/FEIBusiness Operations
    Dan Mor514523067manufacture(74680-101)
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!