LANCOME PARIS RENERGIE LIFT MULTIACTION ULTRA LIFTING FIRMING DARK SPOT CORRECTING BROAD SPECTRUM SPF 30 SUNSCREEN- avobenzone, octisalate and octocrylene cream

Lancome Paris Renergie Lift MultiAction Ultra Lifting Firming Dark Spot Correcting Broad Spectrum SPF 30 Sunscreen by

Drug Labeling and Warnings

Lancome Paris Renergie Lift MultiAction Ultra Lifting Firming Dark Spot Correcting Broad Spectrum SPF 30 Sunscreen 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]

Active ingredients

Avobenzone 3%

Octisalate 5%

Octocrylene 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

Flammable until dry.

Do not use near fire, flame or heat.

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:
● 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 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, isononyl isononanoate, propanediol, vinyl dimethicone/methicone silsesquioxane crosspolymer, alcohol denat., bis-PEG-18 methyl ether dimethyl silane, polyglyceryl-6 distearate, jojoba esters, tocopherol, limnanthes alba (meadowfoam) seed oil, acacia decurrens flower wax, guanosine, cyathea medullaris leaf extract, sodium hyaluronate, hydrolyzed linseed extract, sodium hydroxide, sodium dodecylbenzenesulfonate, sodium benzoate, RED 33, sodium levulinae, phenoxyethanol, adenosine, PEG-8 laurate, helianthus annuus (sunflower) seed wax, polyglyceryl-3 beeswax, polyglycerin-3, ammonium acryloyldimethyltaurae/steareth-25 methacrylate crosspolymer, dimethicone/vinyl dimethicone crosspolyer, dimethiconol, limonene, xanthan gum, benzyl alcohol, cinnamic acid, leontopodium alpinum flower/leaf extract, capryloyl salicylic acid, caprylyl glycol, geraniol, disodium stearoyl glutamate, disodium EDTA, cetyl alcohol, citric acid, potassium sorbate, sculellaria baicalensis root extract, levulinic acid, styrene/acrylaes copolymer, clyberyl caprylate, fragrance

Questions or comments?

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LANCOME PARIS RENERGIE LIFT MULTIACTION ULTRA LIFTING FIRMING DARK SPOT CORRECTING BROAD SPECTRUM SPF 30 SUNSCREEN 
avobenzone, octisalate and octocrylene cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49967-726
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)
GLYCERIN (UNII: PDC6A3C0OX)
DIMETHICONE (UNII: 92RU3N3Y1O)
ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
PROPANEDIOL (UNII: 5965N8W85T)
VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER (UNII: 9NH1UDD2RR)
ALCOHOL (UNII: 3K9958V90M)
BIS-PEG-18 METHYL ETHER DIMETHYL SILANE (UNII: OEB4R3WW9C)
POLYGLYCERYL-6 DISTEARATE (UNII: Z35I17EQOP)
HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)
TOCOPHEROL (UNII: R0ZB2556P8)
MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y)
ACACIA DECURRENS FLOWER WAX (UNII: AU6XZE9IY9)
GUANOSINE (UNII: 12133JR80S)
CYATHEA MEDULLARIS LEAF (UNII: G65ROR2RKA)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)
SODIUM BENZOATE (UNII: OJ245FE5EU)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
SODIUM LEVULINATE (UNII: VK44E1MQU8)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ADENOSINE (UNII: K72T3FS567)
PEG-8 LAURATE (UNII: 762O8IWA10)
POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)
DIMETHICONOL (100000 CST) (UNII: OSA9UP217S)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
XANTHAN GUM (UNII: TTV12P4NEE)
BENZYL ALCOHOL (UNII: LKG8494WBH)
CINNAMIC ACID (UNII: U14A832J8D)
LEONTOPODIUM NIVALE SUBSP. ALPINUM FLOWERING TOP (UNII: QQC1AK06RK)
CAPRYLOYL SALICYLIC ACID (UNII: 5F7PJF6AA4)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
GERANIOL (UNII: L837108USY)
DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)
EDETATE DISODIUM (UNII: 7FLD91C86K)
CETYL ALCOHOL (UNII: 936JST6JCN)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
LEVULINIC ACID (UNII: RYX5QG61EI)
STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A)
GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49967-726-01	1 in 1 CARTON	10/28/2019
1		50 g in 1 JAR; Type 0: Not a Combination Product
2	NDC: 49967-726-02	5 g in 1 JAR; Type 0: Not a Combination Product	10/28/2019
3	NDC: 49967-726-03	1 g in 1 PACKET; Type 0: Not a Combination Product	10/28/2019
4	NDC: 49967-726-04	1 in 1 CARTON	10/28/2019
4		75 g in 1 JAR; Type 0: Not a Combination Product
5	NDC: 49967-726-05	1 in 1 CARTON	10/28/2019
5		30 g in 1 JAR; Type 0: Not a Combination Product
6	NDC: 49967-726-06	1 in 1 CARTON	10/28/2019
6		15 g in 1 JAR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	10/28/2019

Labeler - L'Oreal USA Products Inc (002136794)

Establishment
Name	Address	ID/FEI	Business Operations
SICOS ET CIE		276993581	manufacture(49967-726)

Establishment
Name	Address	ID/FEI	Business Operations
SOCOPLAN		276221405	pack(49967-726)