Label: NORO-X FOAMING HANDSOAP- o-cymen-5-ol soap

  • 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 February 21, 2023

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  • Active ingredients

    o-Cymen-5-ol 0.095%

  • Purposes

    o-Cymen-5-ol 0.095%............................................ Antibacterial

  • Uses

    Uses for hand washing to decrease bacteria on the skin

  • Warnings

    Warnings For external use only.

  • Warnings

    When using this product, avoid contact with eyes. In case of contact with eyes, rinse with water.

  • Warnings

    Stop use and ask a doctor if irritation or redness develops.

  • Warnings

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

  • Directions

    • pump into hands

    • lather with soap for at least 30 seconds

    • rinse hands with water

  • Inactive ingredients

    Water, Disodium Laureth Sulfosuccinate, Glycerin, Cocamidopropyl Betaine, Disodium Cocoamphodiacetate, Lauryl Glucoside,
    Sodium Chloride, Capiylyi Glycol, Ethyihexylglycerin, Menthol, Fragrance, Allantoin, Sodium Benzoate, Citric Acid, Bacillus/Canavalia Ensiformis Seed Ferment Extract, Disodium EDTA, Hexylene Glycol, Butylene Glycol, Chrysanthellum Indicum Extract,
    RhusSemialata Gall Extract, Propolis Extract, Pinus Densiflora Leaf Extract, Scutellaria Baicalensis Root Extract

  • Display Panel

    500mL_label

  • INGREDIENTS AND APPEARANCE
    NORO-X FOAMING HANDSOAP 
    o-cymen-5-ol soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77935-507
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    O-CYMEN-5-OL (UNII: H41B6Q1I9L) (O-CYMEN-5-OL - UNII:H41B6Q1I9L) O-CYMEN-5-OL0.095 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    CHRYSANTHELLUM INDICUM TOP (UNII: STJ856D1Z0)  
    MENTHOL (UNII: L7T10EIP3A)  
    ALLANTOIN (UNII: 344S277G0Z)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    PINUS DENSIFLORA LEAF (UNII: Q1Q9P50WIY)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)  
    PROPOLIS WAX (UNII: 6Y8XYV2NOF)  
    SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)  
    RHUS CHINENSIS GALL (UNII: 4W3Y2V7J3R)  
    CANAVALIA ENSIFORMIS WHOLE (UNII: U485ST9OUN)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77935-507-01500 mL in 1 BOTTLE; Type 0: Not a Combination Product12/27/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other12/27/2022
    Labeler - BIO3S Co.,Ltd. (694813103)
    Registrant - BIO3S Co.,Ltd. (694813103)
    Establishment
    NameAddressID/FEIBusiness Operations
    BIO3S Co.,Ltd.694813103manufacture(77935-507)