Lancome Paris Absolue Revitalizing Brightening Velvet Sunscreen Broad Spectrum SPF 15 by L'Oreal USA Products Inc / SICOS ET CIE / SOCOPLAN Drug Facts

Lancome Paris Absolue Revitalizing Brightening Velvet Sunscreen Broad Spectrum SPF 15 by

Drug Labeling and Warnings

Lancome Paris Absolue Revitalizing Brightening Velvet Sunscreen Broad Spectrum SPF 15 by is a Otc medication manufactured, distributed, or labeled by L'Oreal USA Products Inc, SICOS ET CIE, SOCOPLAN. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

LANCOME PARIS ABSOLUE REVITALIZING BRIGHTENING VELVET SUNSCREEN BROAD SPECTRUM SPF 15- avobenzone, homosalate, octisalate and octocrylene cream 
L'Oreal USA Products Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredientS

Avobenzone 3%

Homosalate 5%

Octisalate 5%

Octrocrylene 7%

Purpose

Sunscreen

Uses

  • helps prevent sunburn

  • if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

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:

● 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

protect the product in this container from excessive heat and direct sun

Inactive ingredients

water, glycerin, dimethicone, silica, PEG-100 stearate, glyceryl stearate, propanediol, glycolic acid, ammonium polyacryloyldimethyl taurate, dicaprylyl carbonate, mica, tocoferol, ascorbyl glucoside, alcohol, sodium hydroxide, sodium hyaluronate, hydrolyzed linseed extract, sodium benzoate, red 4, stearic acid, phenoxyethanol, steareth-100, phenylethyl resorcinol, paeonia albiflora root extract, trisodium ethylenediamine disuccinate, palmitic acid, poloxamer 338, yellow 5, dimethicone/vinyl dimethicone crosspolymer, limonene, xanthan gum, pentaerythrityl tetra-di-t-butyl hydroxyhydrocinnamate, linalool, tin oxide, caprylyl glycol, capryloyl salicylic acid, acrylates/c10-30 alkyl acrylate crosspolymer, myristic acid, geraniol, rose extract, rosa meichibon/delgramaue callus rosa damascena flower oil, rosa centifolia flower extract, butyrospermum parkii (shea) butter, titanium dioxide, tetrasodium glutamate diacetate, citronellol, citric acid, coumarin, fragrance

Questions or comments?

1-800-LANCOME

(1-800-526-2663)

Monday - Friday (9 a.m. - 5 p.m. EST)

image of a carton

LANCOME PARIS ABSOLUE REVITALIZING BRIGHTENING VELVET SUNSCREEN BROAD SPECTRUM SPF 15 
avobenzone, homosalate, octisalate and octocrylene cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 49967-467
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 min  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)  
PROPANEDIOL (UNII: 5965N8W85T)  
GLYCOLIC ACID (UNII: 0WT12SX38S)  
AMMONIUM POLYACRYLOYLDIMETHYL TAURATE (55000 MPA.S) (UNII: F01RIY4371)  
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
MICA (UNII: V8A1AW0880)  
TOCOPHEROL (UNII: R0ZB2556P8)  
ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)  
ALCOHOL (UNII: 3K9958V90M)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
STEARETH-100 (UNII: 4OH5W9UM87)  
PHENYLETHYL RESORCINOL (UNII: G37UFG162O)  
PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P)  
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)  
PALMITIC ACID (UNII: 2V16EO95H1)  
POLOXAMER 338 (UNII: F75JV2T505)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)  
LIMONENE, (+)- (UNII: GFD7C86Q1W)  
XANTHAN GUM (UNII: TTV12P4NEE)  
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)  
LINALOOL, (+/-)- (UNII: D81QY6I88E)  
STANNIC OXIDE (UNII: KM7N50LOS6)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
CAPRYLOYL SALICYLIC ACID (UNII: 5F7PJF6AA4)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
MYRISTIC ACID (UNII: 0I3V7S25AW)  
GERANIOL (UNII: L837108USY)  
ROSA X DAMASCENA FLOWER OIL (UNII: 18920M3T13)  
ROSA CENTIFOLIA FLOWER (UNII: CS4TE8FF7O)  
SHEA BUTTER (UNII: K49155WL9Y)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)  
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
COUMARIN (UNII: A4VZ22K1WT)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 49967-467-011 in 1 CARTON07/18/201901/24/2023
160 mL in 1 JAR; Type 0: Not a Combination Product
2NDC: 49967-467-021 mL in 1 PACKET; Type 0: Not a Combination Product07/18/201901/24/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35207/18/201901/24/2023
Labeler - L'Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIBusiness Operations
SICOS ET CIE276993581manufacture(49967-467) , pack(49967-467)
Establishment
NameAddressID/FEIBusiness Operations
SOCOPLAN276221405pack(49967-467)

Revised: 1/2023