Label: REVITAL PERFECTING DUAL AMPOULE- niacinamide solution

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated August 20, 2015

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  • ACTIVE INGREDIENT

    Active Ingredient: Niacinamide 2.0%

  • INACTIVE INGREDIENT

    Inactive Ingredients Ampoule 1: Water, Camellia Sinensis Leaf Extract, Glycerin, Human Stem Cell Conditioned Media, Glyceryl Citrate/Lactate/Linoleate/Oleate, Olive Europaea (Olive) Fruit Oil, Polysorbate 60, 1,2-Hexanediol, Caprylyl Glycol, Tropolone, Butylene Glycol

    Inactive Ingredients Ampoule 2: Water, Glycerin, PEG/PPG-17/6 Copolymer, Dipropylene Glycol, Glycereth-26, Butylene Glycol, Bis-PEG-18 Methyl Ether Dimethyl Silane, Human Stem Cell Conditioned Media, Glyceryl Citrate/Lactate/Linoleate/Oleate, Olive Europaea (Olive) Fruit Oil, Polysorbate 60, 1,2-Hexanediol, Caprylyl Glycol, Tropolone, Camellia Japonica Flower Extract, Sodium Hyaluronate, Carbomer, Xanthan Gum, Ammonium Acryloyldimethyltaurate/VP Copolymer, Arginine, Adenosine, PEG-60 Hydrogenated Castor Oil, Dimethicone, Phenoxyethanol, Disodium EDTA, Fragrance

  • PURPOSE

    Purpose: Skin Protectant

  • WARNINGS

    Warnings:

    1. For external use only. 2. Avoid contact with eyes and mouth. 3. Discontinue use if signs of irritation or rashes appear. 4. Replace the cap after use. 5.Keep out of reach of babies and children.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of babies and children.

  • INDICATIONS & USAGE

    Indications & Usage: Take a proper amount of the serum, and spread it outward from the inward of the face and Tap the skin lightly for absorption.

  • DOSAGE & ADMINISTRATION

    Dosage & Administration: Take a proper amount of product, and spread it evenly over the entire face.

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    REVITAL PERFECTING DUAL AMPOULE 
    niacinamide solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70038-010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide0.4 mg  in 20 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Glycerin (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70038-010-0120 mL in 1 CARTON; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/10/2015
    Labeler - RAONBIO CORP (689517161)
    Registrant - RAONBIO CORP (689517161)
    Establishment
    NameAddressID/FEIBusiness Operations
    RAONBIO CORP689517161manufacture(70038-010)
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