Label: NYMPHSYN FACE MASK- glycerin cream

  • Category: HUMAN OTC DRUG LABEL

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Drug Label Information

Updated March 21, 2017

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  • ACTIVE INGREDIENT

    Active ingredients: GLYCERIN 2.8%

  • INACTIVE INGREDIENT

    Inactive ingredients: AQUA (WATER), BUTYLENE GLYCOL, CAPRYLIC/CAPRIC TRIGLYCERIDE, COCO-CAPRYLATE/CAPRATE, C12-20 ACID PEG-8 ESTER, POTASSIUM CETYL PHOSPHATE, PHENOXYETHANOL, CI 77891 (TITANIUM DIOXIDE), CARBOMER, POLYACRYLAMIDE, SODIUM POTASSIUM ALUMINUM SILICATE, ETHYLHEXYLGLYCERIN, C13-14 ISOPARAFFIN, CHONDRUS CRISPUS POWDER (CARRAGEENAN), CARAMEL, SODIUM HYDROXIDE, MICA, PARFUM (FRAGRANCE), DISODIUM EDTA, SILICA, LAURETH-7, PEG-8, TRITICUM VULGARE (WHEAT) PROTEIN, PENTYLENE GLYCOL, SODIUM HYALURONATE, TETRADECYL AMINOBUTYROYLVALYLAMINOBUTYRIC UREA TRIFLUOROACETATE TOCOPHEROL, ASCORBYL PALMITATE, MAGNESIUM CHLORIDE, ASCORBIC ACID, CITRIC ACID, NICOTIANA SYLVESTRIS LEAF CELL CULTURE

  • PURPOSE

    Purpose: Skin firming and remodeling

  • WARNINGS

    Warnings: For external use only Avoid contact with eyes. 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: Use one to three times a week

  • DOSAGE & ADMINISTRATION

    Dosage & Administration: - Apply a generous, even layer to clean skin - Leave on for 5 to 10 minutes, then wash-off or leave on over-night

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    NYMPHSYN FACE MASK 
    glycerin cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71276-030
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN1.4 g  in 50 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71276-030-021 in 1 CARTON03/02/2017
    1NDC:71276-030-0150 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(71276-030)
    Establishment
    NameAddressID/FEIBusiness Operations
    U-LAB Switzerland AG485958743manufacture(71276-030)
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