NDC | 49967-636-01, 49967-636-02, 49967-636-03 |
Set ID | 59f0ddf0-f4af-4feb-b64e-57c575843c93 |
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
- Flammable until dry.
- 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
● 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
cyclohexasiloxane, dimethicone, isododecane, alcohol denat., vinyl dimethicone/methicone silsesquioxane crosspolymer, phenyl trimethicone, PEG-10 dimethicone, disteardimonium hectorite, rosa canina fruit oil, tin oxide, ruscus aculeatus root extract, water, silica silylate, aluminum hydroxide, magnesium silicate, disodium stearoyl glutamate, propylene carbonate, synthetic fluophlogopite, tocopheryl acetate, fragrance, linalool, limonene, hydroxyisohexyl 3-cyclohexene carboxaldehyde, butylphenyl methylpropional, hexyl cinnamal; may contain: titanium dioxide, iron oxides
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
LANCOME PARIS NUDE MIRACLE BROAD SPECTRUM SPF 15 SUNSCREEN
octinoxate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-636 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Octinoxate (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) Octinoxate 30 mg in 1 mL Inactive Ingredients Ingredient Name Strength CYCLOMETHICONE 6 (UNII: XHK3U310BA) DIMETHICONE (UNII: 92RU3N3Y1O) ISODODECANE (UNII: A8289P68Y2) ALCOHOL (UNII: 3K9958V90M) PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R) PEG-14 DIMETHICONE (UNII: G7DL1Y4G26) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) ROSA CANINA FRUIT OIL (UNII: CR7307M3QZ) STANNIC OXIDE (UNII: KM7N50LOS6) RUSCUS ACULEATUS ROOT (UNII: ZW12V95I1Q) WATER (UNII: 059QF0KO0R) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) MAGNESIUM SILICATE (UNII: 9B9691B2N9) DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M) PROPYLENE CARBONATE (UNII: 8D08K3S51E) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) LINALOOL, (+/-)- (UNII: D81QY6I88E) LIMONENE, (+)- (UNII: GFD7C86Q1W) HYDROXYISOHEXYL 3-CYCLOHEXENE CARBOXALDEHYDE (UNII: QUE43B9Z2Q) BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FERRIC OXIDE RED (UNII: 1K09F3G675) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-636-01 1 in 1 CARTON 01/01/2014 1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:49967-636-02 1 mL in 1 PACKET; Type 0: Not a Combination Product 01/01/2014 3 NDC:49967-636-03 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/01/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 01/01/2014 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations SICOS ET CIE 276993581 manufacture(49967-636)