Label: DR. DREAM ADVANCED FACIAL TREATMENT TONER- 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 August 24, 2012

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  • ACTIVE INGREDIENT

    witch hazel
  • INACTIVE INGREDIENT

    bis-PEG-18 methyl ether dimethyl silane, butylene glycol, panthenol, sodium PCA, caprylyl glycol, torreya nucifera extract, cornus kousa extract, rosa multiflora fruit extract, chloranthus glaber extract, musa basjoo extract, musa basjoo extract, rh-oligopeptide-1, acetyl hexapeptide=8, palmitoyl oligopeptice, palmitoyl tetrapeptide-7, polysorbate 80, glycerin, caprylhydroxamic acid, adenosine, ammonium acryloyldimethyltaurate, hydroxyethylcellulose, pentylene glycol, cellulose gum, sodium chondroitin sulfate, lavandula angustifolia oil, cymbopogon schoenanthus oil, abies sibirica oil, citrus auratium dulcis peel oil, amyris balsamifera bark oil, salvia sclarea oil, lecithin, sodium phosphate, sodium hyaluronate, rh-polypeptide-60, rh-polypeptide-9, rh-polypeptide-11, rh-polypeptide-2, rh-polypeptide-1, rh-polypeptide-10, copper tripeptide-1, palmitoyl pentapeptide-4, glycine, glutamine, lysine, leucine, methionine, valine, serine, cysteine, cystine, asparagine, alanine, arginine, ornithine, isoleucine,tyrosine, threonine, tryptophan, phenylalanine, proline, histidine
  • PURPOSE

    anti wrinkle
  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children
  • INDICATIONS & USAGE

    after cleaning up your face with clean water apply proper amount to your skin and massage a few minutes
  • 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 ADVANCED FACIAL TREATMENT TONER  
    witch hazel liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53077-1001
    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
    BIS-PEG-18 METHYL ETHER DIMETHYL SILANE (UNII: OEB4R3WW9C)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    TORREYA NUCIFERA WHOLE (UNII: 91Z68135ZV)  
    ROSA DAMASCENA FLOWER OIL (UNII: 18920M3T13)  
    MUSA BASJOO WHOLE (UNII: V3AYC3JL9Y)  
    ACETYL HEXAPEPTIDE-8 (UNII: L4EL31FWIL)  
    PALMITOYL OLIGOPEPTIDE (UNII: HO4ZT5S86C)  
    PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)  
    ADENOSINE (UNII: K72T3FS567)  
    AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)  
    NEOPENTYL GLYCOL (UNII: QI80HXD6S5)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    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:53077-1001-1100 mL in 1 BOTTLE, GLASS
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34708/24/2012
    Labeler - Dr. Dream Inc (557821161)
    Registrant - Dr. Dream Inc (557821161)
    Establishment
    NameAddressID/FEIBusiness Operations
    New & New Co., Ltd557821160manufacture(53077-1001)