Label: LANCOME PARIS RENERGIE LIFT MULTIACTION ULTRA FIRMING AND DARK SPOT CORRECTING MOISTURIZER BROAD SPECTRUM SPF 30 SUNSCREEN- avobenzone, homosalate, octisalate and octocrylene lotion
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NDC Code(s):
49967-768-01,
49967-768-02,
49967-768-03,
49967-768-04, view more49967-768-05
- Packager: L'Oreal USA Products Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 30, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
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Directions
For sunscreen use:
- apply generously and evenly 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 of 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
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Inactive ingredients
water, glycerin, dimethicone, silica, PEG-100 stearate, glyceryl stearate, glycolic acid, guanosine, cyathea medullaris leaf extract, t-butyl alcohol, dicaprylyl carbonate, mica, tocopherol, ascorbyl glycoside, sodium hydroxide, sodium hyaluronate, hydrolyzed linseed extract, sodium benzoate, sodium levulinate, stearic acid, phenoxyethanol, steareth-100, phenylethyl resorcinol, palmitic acid, ammonium polyacryloyldimethyl taurate, dimethicone/vinyl dimethicone crosspolymer, limonene, xanthan gum, pentaerythrityl tetra-di-t-butyl hydroxyhydrocinnamate, benzyl alcohol, tin oxide, cinnamic acid, leontopodium alpinum extract, caprylyl glycol, myristic acid, geraniol, disodium EDTA, titanium dioxide, retinyl palmitate, citric acid, potassium sorbate, levulinic acid, glyceryl pacrylate, fragrance
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
LANCOME PARIS RENERGIE LIFT MULTIACTION ULTRA FIRMING AND DARK SPOT CORRECTING MOISTURIZER BROAD SPECTRUM SPF 30 SUNSCREEN
avobenzone, homosalate, octisalate and octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-768 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX) Avobenzone 30 mg in 1 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 50 mg in 1 mL Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate 50 mg in 1 mL Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM) Octocrylene 70 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) DIMETHICONE (UNII: 92RU3N3Y1O) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) PEG-100 STEARATE (UNII: YD01N1999R) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) GLYCOLIC ACID (UNII: 0WT12SX38S) GUANOSINE (UNII: 12133JR80S) CYATHEA MEDULLARIS LEAF (UNII: G65ROR2RKA) TERT-BUTYL ALCOHOL (UNII: MD83SFE959) DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) MICA (UNII: V8A1AW0880) TOCOPHEROL (UNII: R0ZB2556P8) ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW) SODIUM HYDROXIDE (UNII: 55X04QC32I) HYALURONATE SODIUM (UNII: YSE9PPT4TH) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM LEVULINATE (UNII: VK44E1MQU8) STEARIC ACID (UNII: 4ELV7Z65AP) PHENOXYETHANOL (UNII: HIE492ZZ3T) STEARETH-100 (UNII: 4OH5W9UM87) PHENYLETHYL RESORCINOL (UNII: G37UFG162O) PALMITIC ACID (UNII: 2V16EO95H1) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ) LIMONENE, (+)- (UNII: GFD7C86Q1W) XANTHAN GUM (UNII: TTV12P4NEE) PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS) BENZYL ALCOHOL (UNII: LKG8494WBH) STANNIC OXIDE (UNII: KM7N50LOS6) CINNAMIC ACID (UNII: U14A832J8D) LEONTOPODIUM NIVALE SUBSP. ALPINUM ROOT (UNII: SDW6SS1K6I) CAPRYLYL GLYCOL (UNII: 00YIU5438U) MYRISTIC ACID (UNII: 0I3V7S25AW) GERANIOL (UNII: L837108USY) EDETATE DISODIUM (UNII: 7FLD91C86K) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) LEVULINIC ACID (UNII: RYX5QG61EI) GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-768-01 1 in 1 CARTON 09/01/2017 09/01/2017 1 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:49967-768-02 1 in 1 CARTON 09/01/2017 09/01/2017 2 5 mL in 1 TUBE; Type 0: Not a Combination Product 3 NDC:49967-768-03 1.5 mL in 1 PACKET; Type 0: Not a Combination Product 09/01/2017 09/01/2017 4 NDC:49967-768-04 1 in 1 CARTON 09/01/2017 09/01/2017 4 75 mL in 1 BOTTLE; Type 0: Not a Combination Product 5 NDC:49967-768-05 1 in 1 CARTON 09/01/2017 5 15 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 09/01/2017 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations L'Oreal USA, Inc. 185931458 manufacture(49967-768) , pack(49967-768)
