NDC | 49967-810-01, 49967-810-02 |
Set ID | 6e886062-5e76-44a2-b70a-c977970ff209 |
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:
● apply generously 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, diemthicone, glycerin, polyglyceryl-4 isostearate, isododecane, PEG-8, nylon-12, propanediol, cetyl PEG/PPG-10/1 dimethicone, hexyl laurate, PEG-20, phenoxyethanol, magnesium sulfate, dimethiconol, caprylyl glycol, disodium stearoyl glutamate, fragrance, panthenol, disteardimonium hectorite, tocopherol, propylene carbonate, aluminum hydroxide, adenosine, rhamnose, chondrus cripus (carrageenan), linalool, alpha-isomethyl ionone, limonene, hydroxypropyl tetrahydropyrantriol, geraniol, citronellol, coumarin; may contain: titanium dioxide, iron oxides
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
YVES SAINT LAURENT YOUTH LIBERATOR SERUM FOUNDATION
octinoxate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-810 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Octinoxate (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) Octinoxate 40 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-810-01 1 in 1 CARTON 1 30 mL in 1 BOTTLE, PUMP 2 NDC:49967-810-02 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 07/01/2013 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations SICOS ET CIE 276993581 manufacture(49967-810)