Home > Drugs A-Z > Yves Saint Laurent Le Teint Touche Eclat

Yves Saint Laurent Le Teint Touche Eclat (L'Oreal USA Products Inc)

Available Formats

Dosage Form Package Information Links
LOTION 1 BOTTLE, PUMP in 1 CARTON (49967-065-01) > 30 mL in 1 BOTTLE, PUMP Label Information

Complete Yves Saint Laurent Le Teint Touche Eclat Information

  • Active ingredient

    Octinoxate 7%

  • 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 as 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:

    • shake well before 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

  • Purpose


  • Inactive ingredients

    water, cyclopentasiloxane, glycerin, dimethicone, PEG-10 dimethicone, sorbitol, bis-PEG/PPG-14/14 dimethicone, dimethicone/polyglycerin-3 crosspolymer, sodium chloride, phenoxyethanol, caprylyl glycol, disteardimonium hectorite, disodium stearoyl glutamate, ethylhexylglycerin, fragrance, aluminum hydroxide, ascorbyl palmitate, dipropylene glycol, isotridecyl isononanoate; may contain: titanium dioxide, iron oxides, bismuth oxychloride

    octinoxate lotion
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-065
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 2.1 mL  in 30 mL
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:49967-065-01 1 in 1 CARTON
    1 30 mL in 1 BOTTLE, PUMP
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part352 06/01/2012
    Labeler - L'Oreal USA Products Inc (002136794)
    Name Address ID/FEI Business Operations
    SICOS ET CIE 276993581 manufacture