Label: ANTI-BACTERIAL SLIME gel

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

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Drug Label Information

Updated August 29, 2020

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  • Active Ingredient(s)

    Silver Solution- 1%

  • Purpose

    Anti-septic

  • Use

    Anti-bacterial slime helps reduce bateria that potentially can cause disease.
    For use when soap and water are not available.

  • Warnings

    For external use only.
    Keep appropriately in container after use.

  • Do not use

    in children less than 3.
    on open skin wounds.

  • WHEN USING

    Keep out of eyes, ears, and mouth.
    in case of contact with eyes, rinse eyes thoroughly with water.

  • STOP USE

    Stop use and ask a doctor if irritation or rash occurs.
    If swallowed, get medical help.

  • KEEP OUT OF REACH OF CHILDREN

  • Directions

    place enough on hands and rub hands together not less than 1- 2 minutes.hands dry.
    Supervise children under 3 years of age when using this product to avoid swallowing.
    anti-bacterial slime can be used over and over and best within 1 months if keep appropriately in container whenever after use.

  • Other information

    store in room temperature ( 25 C/77 F )
    avoid freezing and excessive heat above 70 C ( 158 F )

  • Inactive ingredients

    Hydroxypropyl Guar, Sodium Borate, Propylene glycol,
    lodopropynyl Butylcarbamate, 2-Phenoxyethanol,
    Diazolidinyl Urea, pigment, silver solution-C, Aqua.

  • Package Label - Principal Display Panel

    78048-013-04 60G78048-013-01 20G78048-013-06 120G78048-013-03 40G78048-013-02 30G78048-013-05 80G

  • INGREDIENTS AND APPEARANCE
    ANTI-BACTERIAL SLIME 
    anti-bacterial slime gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78048-013
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SILVER CATION (UNII: 57N7B0K90A) (SILVER CATION - UNII:57N7B0K90A) SILVER CATION1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    GUARAPROLOSE (3500 MPA.S AT 1%) (UNII: 3A1I7376TC)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78048-013-0120 g in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
    2NDC:78048-013-0230 g in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
    3NDC:78048-013-0340 g in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
    4NDC:78048-013-0460 g in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
    5NDC:78048-013-0580 g in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
    6NDC:78048-013-06120 g in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other03/30/2020
    Labeler - Dongguan City Dexu Toys Co., Ltd. (403382659)
    Establishment
    NameAddressID/FEIBusiness Operations
    Dongguan City Dexu Toys Co., Ltd.403382659manufacture(78048-013)
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