Label: IBEALEE DARK SPOT CORRECTOR CREAM cream

  • NDC Code(s): 83809-016-01, 83809-016-02
  • Packager: Shenzhen Yikai Electronic Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 27, 2023

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  • Active Ingredient

    Niacinamide 5%

  • Purpose

    Dark Spot Corrector

  • Warnings

    WARNINGS:Keep out of reach of children. For external use only. Before using, test for sensitivity on a small area of skin.

  • Do not use

    Do not use on damaged skin. Use only as directed. Avoid contact with eyes. Rinse with warm water to remove. Stop use and consult your physician if rash occurs. Do not ingest. If swallowed, get medical help or contact a Poison Control Center right away! Do not use if safety sealis broken or missing. Store in a cool, dry place.

  • Keep Oot Of Reach Of Children

    Keep out of reach of children

  • Directions

    Cleanse the application area and pat dry. Gently massage a thin layer into the affected area of skin until fully absorbed. Protect treated skin from sunlight by following up with an SPF 30+ sunscreen.

  • Inactive ingredients

    Water, Sunflower Oil, Caprylyl Caprylate/Caprate,Glycerin,Trideceth-6, Aloe Vera, Niacinamide, Glycyrrhiza Glabra Extract, Morus Alba Root Extract, Hydrolyzed Oat Protein,Ethyl Ascorbic Acid, Alpha Arbutin, Hyaluronic Acid, Phenoxyethanol,Green Tea Extract, Tetrapeptide-21, Potassium Sorbate, Citric Acid,Xanthan Gum, Tocopherol, Soy Isoflavones, Cistus Ladaniferus Oil,Lemon Essential Oil.

  • Use

    Remove dark spots on face.

  • PRINCIPAL DISPLAY PANEL

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  • INGREDIENTS AND APPEARANCE
    IBEALEE DARK SPOT CORRECTOR CREAM 
    ibealee dark spot corrector cream cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83809-016
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    TRIDECETH-6 (UNII: 3T5PCR2H0C)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    3-O-ETHYL ASCORBIC ACID (UNII: 6MW60CB71P)  
    ALPHA-ARBUTIN (UNII: 72VUP07IT5)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)  
    MORUS ALBA ROOT (UNII: CST1G9BZGD)  
    CAPRYLYL CAPRYLATE/CAPRATE (UNII: 22MCG4RSMR)  
    GELATIN HYDROLYSATE (PORCINE SKIN, MW 3000) (UNII: 0K9R94573C)  
    HYALURONIC ACID (UNII: S270N0TRQY)  
    TETRAPEPTIDE-21 (UNII: 179JUC43HU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83809-016-0120 g in 1 CANISTER; Type 0: Not a Combination Product12/26/2023
    2NDC:83809-016-0250 g in 1 CANISTER; Type 0: Not a Combination Product12/26/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01612/26/2023
    Labeler - Shenzhen Yikai Electronic Technology Co., Ltd. (700426808)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Yikai Electronic Technology Co., Ltd.700426808label(83809-016) , manufacture(83809-016)
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