NDC | 49967-064-01, 49967-064-02, 49967-064-03 |
Set ID | 0600c8a9-fcf7-4f1e-a6c2-4726fd159d1e |
Category | HUMAN OTC DRUG LABEL |
Packager | L'Oreal USA Products Inc |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- Active ingredient
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
-
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
-
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
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
YVES SAINT LAURENT LE TEINT TOUCHE ECLAT ILLUMINATING FOUNDATION BROAD SPECTRUM SPF 19 SUNSCREEN
octinoxate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-064 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 70 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-064-01 1 in 1 CARTON 1 30 mL in 1 BOTTLE, PUMP 2 NDC:49967-064-02 1 in 1 CARTON 2 10 mL in 1 BOTTLE 3 NDC:49967-064-03 1 mL in 1 PACKET 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) Establishment Name Address ID/FEI Business Operations SICOS ET CIE 276993581 manufacture(49967-064)