Label: DR. DREAM HYDRAMEMORY DEEP CLEANSING- witch hazel liquid

  • 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 September 25, 2012

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  • ACTIVE INGREDIENT

    witch hazel
  • INACTIVE INGREDIENT

    water, myristic acid, glycerin, butylene glycol, potassium hydroxide, stearic acid, lauryl betaine, lauric acid, cocamide dea, potassium cocoyl glycinate, sodium methyl cocoyl taurate, polyquaternium-7, glyceryl stearate, clycol stearate, bambusa vulgaris sap extract, betula alba juice, panthenol, sea water, orange peel oil, caprylyl glycol, disodium edta, betaine, caprylhydroxamic acid, bergamot fruit oil, pelargonium graveolens flower oil, cananga odorata flower oil, sodium hyaluronate
  • PURPOSE

    general care
  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children
  • INDICATIONS & USAGE

    Carry out cleansing, as if you massage your entire face using foam, and then sufficiently rinse your face with warm water, after taking out the proper amount to your palm and making foams with soft and warm water. It would be much better to apply patting with cold water to your face while you are rinsing your face in the end.
  • WARNINGS

    When using this product
    - keep out of eyes, ears, and mouth.  If contact occurs, rinse with plenty of cold water right away and contact a physician.  If swallowing, drink plenty of water and contact a physician
  • DOSAGE & ADMINISTRATION

    for external use only
  • PRINCIPAL DISPLAY PANEL

    package label
  • INGREDIENTS AND APPEARANCE
    DR. DREAM HYDRAMEMORY DEEP CLEANSING 
    witch hazel liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53077-9001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL0.1 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    MUSA BASJOO WHOLE (UNII: V3AYC3JL9Y)  
    ACETYL HEXAPEPTIDE-8 (UNII: L4EL31FWIL)  
    PALMITOYL OLIGOPEPTIDE (UNII: HO4ZT5S86C)  
    PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)  
    ADENOSINE (UNII: K72T3FS567)  
    AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)  
    NEOPENTYL GLYCOL (UNII: QI80HXD6S5)  
    BLACK OLIVE (UNII: 2M6QWV94OC)  
    SODIUM CHONDROITIN SULFATE (PORCINE; 5500 MW) (UNII: H5BJH23Z9A)  
    LAVANDULA ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P)  
    CYMBOPOGON SCHOENANTHUS OIL (UNII: XE7K568ILO)  
    ABIES SIBIRICA LEAF OIL (UNII: XRY0V4VZKZ)  
    ORANGE (UNII: 5EVU04N5QU)  
    AMYRIS BALSAMIFERA OIL (UNII: I1BJ961J2E)  
    CLARY SAGE OIL (UNII: 87L0D4U3M0)  
    LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
    SODIUM PHOSPHATE (UNII: SE337SVY37)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    THIOREDOXIN (UNII: XJZ418133Z)  
    PREZATIDE COPPER (UNII: 6BJQ43T1I9)  
    PALMITOYL PENTAPEPTIDE-4 (UNII: KK181SM5JG)  
    GLYCINE (UNII: TE7660XO1C)  
    GLUTAMINE (UNII: 0RH81L854J)  
    LYSINE (UNII: K3Z4F929H6)  
    LEUCINE (UNII: GMW67QNF9C)  
    METHIONINE (UNII: AE28F7PNPL)  
    VALINE (UNII: HG18B9YRS7)  
    SERINE (UNII: 452VLY9402)  
    CYSTEINE (UNII: K848JZ4886)  
    CYSTINE (UNII: 48TCX9A1VT)  
    ASPARAGINE (UNII: 5Z33R5TKO7)  
    ALANINE (UNII: OF5P57N2ZX)  
    ARGININE (UNII: 94ZLA3W45F)  
    ORNITHINE (UNII: E524N2IXA3)  
    ISOLEUCINE (UNII: 04Y7590D77)  
    TYROSINE (UNII: 42HK56048U)  
    THREONINE (UNII: 2ZD004190S)  
    TRYPTOPHAN (UNII: 8DUH1N11BX)  
    PHENYLALANINE (UNII: 47E5O17Y3R)  
    PROLINE (UNII: 9DLQ4CIU6V)  
    HISTIDINE (UNII: 4QD397987E)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53077-9001-1120 mL in 1 TUBE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34709/25/2012
    Labeler - Dr. Dream Inc (557821161)
    Registrant - Dr. Dream Inc (557821161)
    Establishment
    NameAddressID/FEIBusiness Operations
    New & New Co., Ltd557821160manufacture(53077-9001)