LANCOME PARIS RENERGIE LIFT MULTIACTION ULTRA FIRMING AND DARK SPOT CORRECTING MOISTURIZER BROAD SPECTRUM SPF 30 SUNSCREEN- avobenzone, homosalate, octisalate and octocrylene lotion 
L'Oreal USA Products Inc

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Drug Facts

Active ingredients

Avobenzone 3%

Homosalate 5%

Octisalate 5%

Octocrylene 7%

Purpose

Sunscreen

Uses

Warnings

For external use only

Do not use

on damaged or broken skin

When using this product

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

rash occurs

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

For sunscreen use:

Other information

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?

1-800-LANCOME (1-800-526-2663) Monday - Friday (9 a.m. - 5 p.m. EST)

image of a label

image of a label
LANCOME PARIS RENERGIE LIFT MULTIACTION ULTRA FIRMING AND DARK SPOT CORRECTING MOISTURIZER BROAD SPECTRUM SPF 30 SUNSCREEN 
avobenzone, homosalate, octisalate and octocrylene lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-768
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX) Avobenzone30 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE50 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate50 mg  in 1 mL
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM) Octocrylene70 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49967-768-011 in 1 CARTON09/01/201709/01/2017
150 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:49967-768-021 in 1 CARTON09/01/201709/01/2017
25 mL in 1 TUBE; Type 0: Not a Combination Product
3NDC:49967-768-031.5 mL in 1 PACKET; Type 0: Not a Combination Product09/01/201709/01/2017
4NDC:49967-768-041 in 1 CARTON09/01/201709/01/2017
475 mL in 1 BOTTLE; Type 0: Not a Combination Product
5NDC:49967-768-051 in 1 CARTON09/01/2017
515 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02009/01/2017
Labeler - L'Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIBusiness Operations
L'Oreal USA, Inc.185931458manufacture(49967-768) , pack(49967-768)

Revised: 12/2023
Document Id: d3fab022-9243-4945-a227-6f20598307d6
Set id: bf0e22df-4043-407f-a930-29595da1bdf6
Version: 7
Effective Time: 20231230
 
L'Oreal USA Products Inc