Label: BAEKNYONDONGAN CHI- witch hazel shampoo

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated May 30, 2012

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  • ACTIVE INGREDIENT

    Active ingredient: WITCH HAZEL 0.1%

  • INACTIVE INGREDIENT

    Inactive ingredients:
    Sodium Laureth sulfate, Water, Perilla Ocymoides Leaf  Extract, Oryza Sativa (Rice) Extract, Butylene Glycol, Ammonium Lauryl Sulfate, Acrylates Copolymer, Cocamidopropyl Betaine, Lauramide DEA, Triethanolamine, Dimethicone, C12-15 Pareth-3, Perfume, Guar Hydroxypropyltrimonium Chloride, Methylparaben, Menthol, Sophora Angustifolia Root Extract, Methylchloroisothiazolinone,  Methylisothiazolinone, Disodium EDTA, Prunus Armeniaca (Apricot) Kernel Extract, Prunus Persica (Peach) Kernel Extract, Angelica Gigas Root Extract, Polygonum Multiflorum Root Extract, Astragalus Membranaceus Root Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Panax Ginseng Root Extract, Cordyceps Sinensis Extract, Eclipta Prostrata Extract, Carthamus Tinctorius (Safflower) Flower Extract

  • PURPOSE

    Purpose: Skin Protectant

  • WARNINGS

    Warnings:
    For external use only.
    Do not use on wounds of if you are allergic to any ingredients of this product.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children:
    Keep away from children.

  • INDICATIONS & USAGE

    Indication and usage:
    Thoroughly wet the scalp.
    Apply a small amount of shampoo to the hair.
    Gently massage your scalp with lather and rinse.

  • DOSAGE & ADMINISTRATION

    Dosage and administration:
    Take appropriate amount according to your hair condition and use it every day.

  • PRINCIPAL DISPLAY PANEL

    Image of bottle

  • INGREDIENTS AND APPEARANCE
    BAEKNYONDONGAN CHI 
    witch hazel shampoo
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54948-110
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL0.55 mL  in 550 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    WATER (UNII: 059QF0KO0R)  
    PERILLA FRUTESCENS LEAF (UNII: T4L5881Y68)  
    AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    LAURIC DIETHANOLAMIDE (UNII: I29I2VHG38)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    MENTHOL (UNII: L7T10EIP3A)  
    SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    PRUNUS ARMENIACA SEED (UNII: 75356789IW)  
    PRUNUS PERSICA SEED (UNII: V9C81470RR)  
    ANGELICA GIGAS ROOT (UNII: 32766B2FHX)  
    FALLOPIA MULTIFLORA ROOT (UNII: AUZ3VD75MC)  
    ASTRAGALUS PROPINQUUS ROOT (UNII: 922OP8YUPF)  
    GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)  
    OPHIOCORDYCEPS SINENSIS (UNII: 8Q1GYP08KU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54948-110-01550 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34708/03/2011
    Labeler - MIX & MATCH CO., LTD. (689898943)
    Registrant - MIX & MATCH CO., LTD. (689898943)
    Establishment
    NameAddressID/FEIBusiness Operations
    MIX & MATCH CO., LTD.689898943manufacture
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