Label: PANDAS DREAM MAGIC- glycerin, niacinamide cream

  • Category: HUMAN OTC DRUG LABEL

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 June 15, 2016

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  • ACTIVE INGREDIENT

    Active ingredient: Glycerin 6.0%, Niacinamide 2.0%

  • INACTIVE INGREDIENT

    Inactive Ingredient: Water, Butylene Glycol, Cyclopentasiloxane, Cyclohexasiloxane, Titanium Dioxide (CI 77891), Alcohol Denat., Cetyl PEG/PPG-10/1 Dimethicone, Sodium Chloride, Phenoxyethanol, Chlorphenesin, Dimethicone/Vinyl Dimethicone Crosspolymer, Ethylhexylglycerin, Fragrance, Caprylyl Glycol, Honey Extract, Phyllostachis Bambusoides Juice, Disodium EDTA, Alcohol

  • PURPOSE

    Purpose: Skin Protectant

  • WARNINGS

    Warnings: For external use only. When using this product do not get into eyes. Stop use and ask a doctor if rash occurs. Do not use on - deep puncture wounds - animal bites - serious burns Keep out of reach of children.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • Use

    Use: Helps prevent and relieve chapped or cracked skin

  • Directions

    Directions: - Clean the skin thoroughly before using - Apply in daily skin care routine

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    PANDAS DREAM MAGIC 
    glycerin, niacinamide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59078-312
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Glycerin (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) Glycerin3.0 g  in 50 g
    Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide1.0 g  in 50 g
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Butylene Glycol (UNII: 3XUS85K0RA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59078-312-021 in 1 CARTON05/01/2016
    1NDC:59078-312-0150 g in 1 CONTAINER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/01/2016
    Labeler - TONYMOLY CO.,LTD (688216798)
    Registrant - TONYMOLY CO.,LTD (688216798)
    Establishment
    NameAddressID/FEIBusiness Operations
    TONYMOLY CO.,LTD688216798manufacture(59078-312)