Label: NATURE CLEAN- citiric acid spray

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

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Drug Label Information

Updated October 23, 2020

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  • ACTIVE INGREDIENT

    Citiric acid 0.01% v/v

  • INACTIVE INGREDIENTS

    Ascorbic acid, Citric extractives, DL-Malic acid, Ethanol, Lactic acid, Water

  • PURPOSE

    Antimicrobial

  • WARNINGS

    For external use only

    When using this product ■ Keep out of eyes. In case of contact with eyes, flush thoroughly with water. ■ Avoid contact with broken skin. ■ Do not inhale or ingest.

    Stop use and ask a doctor if skin irritation or rash develops.

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

  • 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.

  • Uses

    ■ Disinfectant to help reduce bacteria on the skin and surfaces
    ■ Recommended for repeated use

  • Directions

    ■ Place enough product on hands to cover all surfaces. Rub hands together until dry.
    ■ Supervise children under 6 years of age when using this product to avoid swallowing.

  • Other information

    ■ Store between 15-30℃(59-86℉)
    ■ Avoid freezing and excessive heat above 40℃(104℉)

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of bottle

  • INGREDIENTS AND APPEARANCE
    NATURE CLEAN 
    citiric acid spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80642-050
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) ANHYDROUS CITRIC ACID0.05 g  in 500 mL
    Inactive Ingredients
    Ingredient NameStrength
    Ascorbic acid (UNII: PQ6CK8PD0R)  
    MALIC ACID (UNII: 817L1N4CKP)  
    ALCOHOL (UNII: 3K9958V90M)  
    Lactic acid (UNII: 33X04XA5AT)  
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80642-050-01500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product10/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/01/2020
    Labeler - Seoul Food Research & Development Co., Ltd. (688787758)
    Registrant - Seoul Food Research & Development Co., Ltd. (688787758)
    Establishment
    NameAddressID/FEIBusiness Operations
    Seoul Food Research & Development Co., Ltd.688787758manufacture(80642-050)
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