Label: LANCOME PARIS RENERGIE LIFT MULTIACTION SUNSCREEN BROAD SPECTRUM SPF 15 LIFT AND FIRMING FACE AND NECK ALL SKIN TYPES- avobenzone, octisalate and octocrylene cream
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NDC Code(s):
49967-633-01,
49967-633-02,
49967-633-03,
49967-633-04, view more49967-633-05, 49967-633-06, 49967-633-07, 49967-633-08
- Packager: L'Oreal USA Products Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 23, 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, dimethicone, glycerin, hydrogenated polyisobutene, beeswax, poly C10-30 alkyl acrylate, yeast extract, guanosine, cyathea medullaris leaf extract, sucrose stearate, secale cereale (rye) seed extract, sodium polyacrylate, sodium hydroxide, red 4, stearic acid, phenoxyethanol, adenosine, PEG-100 stearate, palmitic acid, silica, chlorphenesin, yellow 5, dimethicone/vinyl dimethicone crosspolymer, dimethiconol, limonene, pentylene glycol, benzyl alcohol, linalool, caprylyl glycol, acrylates/C10-30 alkyl acrylate crosspolymer, disodium stearoyl glutamate, disodium EDTA, citronellol, aluminum starch octenylsuccinate, coumarin, glyceryl stearate, fragrance
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
LANCOME PARIS RENERGIE LIFT MULTIACTION SUNSCREEN BROAD SPECTRUM SPF 15 LIFT AND FIRMING FACE AND NECK ALL SKIN TYPES
avobenzone, octisalate and octocrylene creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-633 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 g Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate 50 mg in 1 g Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM) Octocrylene 70 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCERIN (UNII: PDC6A3C0OX) HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ) YELLOW WAX (UNII: 2ZA36H0S2V) YEAST, UNSPECIFIED (UNII: 3NY3SM6B8U) GUANOSINE (UNII: 12133JR80S) CYATHEA MEDULLARIS LEAF (UNII: G65ROR2RKA) SUCROSE STEARATE (UNII: 274KW0O50M) SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J) SODIUM HYDROXIDE (UNII: 55X04QC32I) FD&C RED NO. 4 (UNII: X3W0AM1JLX) STEARIC ACID (UNII: 4ELV7Z65AP) PHENOXYETHANOL (UNII: HIE492ZZ3T) ADENOSINE (UNII: K72T3FS567) PEG-100 STEARATE (UNII: YD01N1999R) PALMITIC ACID (UNII: 2V16EO95H1) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CHLORPHENESIN (UNII: I670DAL4SZ) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ) DIMETHICONOL (100000 CST) (UNII: OSA9UP217S) LIMONENE, (+)- (UNII: GFD7C86Q1W) PENTYLENE GLYCOL (UNII: 50C1307PZG) BENZYL ALCOHOL (UNII: LKG8494WBH) LINALOOL, (+/-)- (UNII: D81QY6I88E) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) COUMARIN (UNII: A4VZ22K1WT) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-633-01 1 in 1 CARTON 12/27/2016 1 75 g in 1 JAR; Type 0: Not a Combination Product 2 NDC:49967-633-02 1 in 1 CARTON 12/27/2016 2 50 g in 1 JAR; Type 0: Not a Combination Product 3 NDC:49967-633-03 1 in 1 CARTON 12/27/2016 3 2 g in 1 JAR; Type 0: Not a Combination Product 4 NDC:49967-633-04 200 g in 1 JAR; Type 0: Not a Combination Product 12/27/2016 5 NDC:49967-633-05 2 g in 1 PACKET; Type 0: Not a Combination Product 12/27/2016 6 NDC:49967-633-06 15 g in 1 JAR; Type 0: Not a Combination Product 12/27/2016 7 NDC:49967-633-07 7 g in 1 PACKET; Type 0: Not a Combination Product 11/09/2018 8 NDC:49967-633-08 1 g in 1 PACKET; Type 0: Not a Combination Product 11/09/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 12/27/2016 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations SICOS ET CIE 276993581 manufacture(49967-633) , pack(49967-633) Establishment Name Address ID/FEI Business Operations L'Oreal USA, Inc. 185931458 manufacture(49967-633)
