Label: NYMPHSYN MAXIMIZER- glycerin cream

  • 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 March 22, 2017

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  • ACTIVE INGREDIENT

    Active ingredients: GLYCERIN 6.29%

  • INACTIVE INGREDIENT

    Inactive ingredients: AQUA (WATER), C12-20 ACID PEG-8 ESTER, CAPRYLIC/CAPRIC TRIGLYCERIDE, BUTYLENE GLYCOL, CYCLOPENTASILOXANE, CETYL ALCOHOL, PHENOXYETHANOL, POTASSIUM CETYL PHOSPHATE DIMETHICONE, CARBOMER, SODIUM POTASSIUM ALUMINUM SILICATE ETHYLHEXYLGLYCERIN, DIMETHICONOL, SODIUM HYDROXIDE, PARFUM (FRAGRANCE), CI 77891 (TITANIUM DIOXIDE), DISODIUM EDTA, MICA, PPG-25-LAURETH-25, SILICA, PALMITOYL TRIPEPTIDE-5, PEG-8, TRITICUM VULGARE (WHEAT) PROTEIN, PENTYLENE GLYCOL, SODIUM HYALURONATE, TOCOPHEROL, ASCORBYL PALMITATE, ASCORBIC ACID, CITRIC ACID, NICOTIANA SYLVESTRIS LEAF CELL CULTURE, SODIUM DEHYDROACETATE, SORBIC ACID, UNDECYLENIC ACID

  • PURPOSE

    Purpose: Moisturizing and lifting for youthful appearance

  • WARNINGS

    Warnings: For external use only Avoid eye contour area Discontinue use if signs of irritation or rashes appear.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • INDICATIONS & USAGE

    Indications & Usage: Apply morning and night

  • DOSAGE & ADMINISTRATION

    Dosage & Administration: Apply morning and night to face and neck after serum and ampoule

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    NYMPHSYN MAXIMIZER 
    glycerin cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71276-060
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN3.14 g  in 50 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    C12-20 ACID PEG-8 ESTER (UNII: 9M7A3K4339)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71276-060-021 in 1 CARTON03/02/2017
    1NDC:71276-060-0150 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other03/02/2017
    Labeler - ULAB (688976692)
    Registrant - ULAB (688976692)
    Establishment
    NameAddressID/FEIBusiness Operations
    ULAB688976692relabel(71276-060)
    Establishment
    NameAddressID/FEIBusiness Operations
    U-LAB Switzerland AG485958743manufacture(71276-060)