Label: LIQUIDGUARD- phosphates liquid

  • Category: HUMAN OTC DRUG LABEL

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Drug Label Information

Updated August 9, 2020

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  • SPL UNCLASSIFIED SECTION

    The liquid guard is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:

    The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.

  • Active Ingredient(s)

    Phosphates 2.5 % v/v. Purpose: Liquid Guard

  • PURPOSE

    Liquid Guard

  • INDICATIONS & USAGE

    Liquid Guard to help reduce bacteria that potentially can cause disease.

  • Warnings

    For external use only. Keep out of reach of eyes, ears, and mouth

  • Do not use

    Keep out od reach of childrens

  • WHEN USING

    When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • STOP USE

    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Place enough product to clean the infected area. Do not use of wet surfaces / skin.

  • STORAGE AND HANDLING

    Store between 15-30C (59-86F)
    Avoid freezing and excessive heat above 40C (104F)

  • Inactive ingredients

    purified water USP

  • Maximum 1000000000 mL in 1 CONTAINER (79836-500-01)

    Label Approved

    5000 mL NDC: 79836-500-01

  • INGREDIENTS AND APPEARANCE
    LIQUIDGUARD 
    phosphates liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79836-500
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PHOSPHATE ION (UNII: NK08V8K8HR) (PHOSPHATE ION - UNII:NK08V8K8HR) PHOSPHATE ION2.5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 98.1 mL  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79836-500-015000 mL 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 - Nano Care Deutschland AG (314463865)
    Registrant - Nano Care Deutschland AG (314463865)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nano Care Deutschland AG314463865manufacture(79836-500)
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