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Yves Saint Laurent Le Teint Touche Eclat Sunscreen Illuminating Foundation SPF 19

Dosage form: lotion
Ingredients: Octinoxate 2.1mL in 30mL
Labeler: L'Oreal USA Products Inc
NDC Code: 49967-065

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Facts

Active ingredient

Octinoxate 7%

  • 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


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.


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



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 TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-065
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Octinoxate (Octinoxate) Octinoxate2.1 mL  in 30 mL
#Item CodePackage Description
1NDC:49967-065-011 BOTTLE, PUMP (BOTTLE) in 1 CARTON
130 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35206/01/2012
Labeler - L'Oreal USA Products Inc (002136794)
SICOS ET CIE276993581manufacture

Revised: 06/2012
L'Oreal USA Products Inc

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.