Label: DR. DREAM HYDRAMEMORY DEEP ACTIVE MOISTURIZER- witch hazel cream

  • 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, cyclopentasiloxane, butylene glycol, betula alba juice, dimethicone, sodium chloride, peg/ppg-18/18 dimethicone, peg/ppg-19/18 dimethicone, olive fruit oil, magnolia kobus bark extract, torreya nucifera extract, cornus kousa extract, rosa multiflora fruit extract, chloranthus glaber extract, musa basjoo extract, acetyl hexapeptide 8, allantoin palmitoyl oligopeptide, palmitoyl tetrapeptide 7, human oligopeptide 1, willow bark extract, carmellia sinensis leaf extract, lavender oil, cymbopogon schoenanthus oil, abies sibirica oil, orange peel oil, amyris balsamifera bark oil, clary oil, grapefruit extract, tocopheryl acetate, propolis extract, thujopsis dolabrata branch extract, matricaria flower/leaf extract
  • PURPOSE

    anti wrinkle care
  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children
  • INDICATIONS & USAGE

    Take out the proper amount with the built-in spatula and apply it to your face as massaging to be well absorbed.
    Especially there would be better effect if you apply it frequently after laser treatment.
  • 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 ACTIVE MOISTURIZER 
    witch hazel cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53077-6001
    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
    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:53077-6001-180 mL in 1 BOTTLE, GLASS
    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(53077-6001)
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