Label: ERBORIAN - BB CREME NUDE SPF20- octinoxate, titanium dioxide, zinc oxide cream

  • NDC Code(s): 10345-902-15, 10345-902-45
  • Packager: LABORATOIRES M&L
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 15, 2023

If you are a consumer or patient please visit this version.

  • Active ingredients

    Octinoxate 3.00% Titanium dioxide 6.28% Zinc oxide 1.92%


  • 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 - . 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






    Sun Protection Measures

  • Inactive Ingredients

    Aqua/water - cyclomethicone- glycerin hexyl laurate - dipropylene glycol - peg-10 dimethicone- talc - dimethicone- isoeicosane-disteardimonium hectorite - betaine -centella asiatica extract- polygonum cuspidatum root extract - scutellaria baicalensis root extract - camellia sinensis leaf extract - glycyrrhiza glabra (licorice) root extract - chamomilla recutita (matricaria) flower extract - portulaca oleracea extract - rosmarinus officinalis (rosemary) leaf extract - hydrogenated starch hydrolysate - ethylhexylglycerin - tocopheryl acetate - magnesium sulfate - silica - glycosyl trehalose - aluminum hydroxide - palmitic acid - stearic acid - butylene glycol - phenoxyethanol - vinyl dimethicone/methicone silsesquioxane crosspolymer - acrylates/dimethicone copolymer - dimethicone/vinyl dimethicone crosspolymer -methicone - CI 77492/iron oxides - CI 77499/iron oxides - CI 77491/iron oxides

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    ERBORIAN - BB CREME NUDE SPF20 
    octinoxate, titanium dioxide, zinc oxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10345-902
    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)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    TALC (UNII: 7SEV7J4R1U)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    ISOEICOSANE (UNII: AR294KAG3T)  
    DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
    BETAINE (UNII: 3SCV180C9W)  
    GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)  
    HYDROGENATED STARCH HYDROLYSATE (UNII: 27F77DSJ5V)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)  
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
    PALMITIC ACID (UNII: 2V16EO95H1)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10345-902-451 in 1 BOX08/17/2016
    145 mL in 1 TUBE; Type 0: Not a Combination Product
    2NDC:10345-902-151 in 1 BOX08/17/2016
    215 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02008/17/2016
    Labeler - LABORATOIRES M&L (262533623)