Label: ERBORIAN - BB CREME AU GINSENG DORE SPF 20- octinoxate, titanium dioxide, zinc oxide cream

  • NDC Code(s): 10345-901-15, 10345-901-45
  • Packager: LABORATOIRES M&L
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 5, 2023

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  • Drug Facts

  • Active ingredients

    Ethylhexyl methoxycinnamate / Octinoxate 3.00%....….......Sunscreen
    Titanium dioxide 6.28%......Sunscreen
    Zinc oxide 1.92%................Sunscreen

    Purpose

    Sunscreen

  • Uses

    • Helps prevent sunburn
    • If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun
  • Warnings

    ​For external use only

    Do not use

    • on damaged or broken skin

    When using this product

    • keep out of eyes.  Rinse with water to remove

    Stop use and ask a doctor if

    rash occurs.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away

  • Directions

    For sunscreen use:

    • Apply liberally 15 minutes before sun exposure
    • Reapply at least every 2 hours
    • Use a water resistant sunscreen if swimming or sweating
    • Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk,  regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
    • Limit time in the sun, especially from 10 a.m. –2 p.m.
    • Wear long-sleeved shirts, pants, hats and sunglasses
    • Children under 6 months of age: Ask a doctor
  • Other information

    • Protect the product in this container from excessive heat and direct sun
  • Inactive ingredients

    Aqua/water - cyclomethicone - glycerin - talc - dipropylene glycolpeg-10 dimethicone - dimethicone - hexyl laurate - CI 77492/iron oxides - disteardimonium hectorite - betaine - isoeicosane - panax ginseng root extract - portulaca oleracea extract - glycyrrhiza glabra (licorice) root extract - dioscorea villosa (wild yam) root extract - kigelia africana fruit extract - equisetum giganteum extract - hydrogenated starch hydrolysate - ethylhexylglycerin - tocopheryl acetate - glycosyl trehalose - magnesium sulfate - aluminum hydroxide - palmitic acid - stearic
    acid - phenoxyethanol - butylene glycol - dimethicone/vinyl dimethicone crosspolymer - methicone - acrylates/dimethicone copolymer -  parfum/fragrance - hexyl cinnamal - alpha-isomethyl ionone - linalool - citronellol - geraniol - eugenol - limonene - CI 77491/iron oxide

  • Questions or comments?

    Call toll free 1-888-975-2162

  • Product Label

    GinsengDore

  • INGREDIENTS AND APPEARANCE
    ERBORIAN - BB CREME AU GINSENG DORE SPF 20 
    octinoxate, titanium dioxide, zinc oxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10345-901
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE30 mg  in 1 mL
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE62.8 mg  in 1 mL
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION19.2 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CYCLOMETHICONE (UNII: NMQ347994Z)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    HEXYL LAURATE (UNII: 4CG9F9W01Q)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
    BETAINE (UNII: 3SCV180C9W)  
    ISOEICOSANE (UNII: AR294KAG3T)  
    ASIAN GINSENG (UNII: CUQ3A77YXI)  
    PURSLANE (UNII: M6S840WXG5)  
    LICORICE (UNII: 61ZBX54883)  
    DIOSCOREA VILLOSA TUBER (UNII: IWY3IWX2G8)  
    KIGELIA AFRICANA FRUIT (UNII: L4J6XXD1E0)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)  
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
    PALMITIC ACID (UNII: 2V16EO95H1)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)  
    ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
    GERANIOL (UNII: L837108USY)  
    EUGENOL (UNII: 3T8H1794QW)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10345-901-151 in 1 BOX02/06/2015
    115 mL in 1 TUBE; Type 0: Not a Combination Product
    2NDC:10345-901-451 in 1 BOX02/06/2015
    245 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02002/06/2015
    Labeler - LABORATOIRES M&L (262533623)
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