RENER LIFT MULTI ACTION ULTRA SPF 30- avobenzone, octisalate, octocrylene cream

Rener lift multi action ultra SPF 30 by

Drug Labeling and Warnings

Rener lift multi action ultra SPF 30 by is a Otc medication manufactured, distributed, or labeled by BPS 60. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts:

Active ingredients:

Avobenzone 3%

Octisalate 5%

Octocrylene 7%

Purpose:

Sunscreen.

Uses

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

Warnings:

For external use only.

Do not use near fire, flame or heat. Flammable until dry. 

Do not use

on damaged or broekn skin

When using this product

keep out of eyes. Rinse with water to remove.

Stop use and 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
• Spending time in the sun increases your risk of skin cancer and early sking 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:  Sun Protection Measures.
• 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, sodium hyaluronate, hydrolyzed linseed extract, sodium hydroxide, sodium dodecylbenzenesulfonate, sodium benzoate, RED 33, phenoxyethanol, adenosine, PEG-8 laurate, helianthus annuus (sunflower) seed wax, polyglyceryl-3 beeswax, polyglycerin-3, ammonium acryloyldimethyltaurate/steareth-25 methacrylate crosspolymer, dimethicone/vinyl dimethicone crosspolymer, dimethiconol, limonene, xanthan gum, benzyl alcohol, leontopodium alpinum flower/leaf extract, capryloyl salicylic acid, caprylyl glycol, geraniol, disodium stearoyl glutamate, disodium EDTA, cetyl alcohol, citric acid, potassium sorbate, scutellaria baicalensis root extract, styrene/acrylates copolymer, fragrance

Questions or comments?

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

Package Labeling:70581-020-04

Package Labeling:70581-020-01

Package Labeling:70581-020-00

Package Labeling:70581-020-02

Package Labeling:70581-020-03

INGREDIENTS AND APPEARANCE

RENER LIFT MULTI ACTION ULTRA SPF 30 
avobenzone, octisalate, octocrylene cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70581-020
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
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)
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)
TOCOPHEROL (UNII: R0ZB2556P8)
MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y)
ACACIA DECURRENS FLOWER WAX (UNII: AU6XZE9IY9)
GUANOSINE (UNII: 12133JR80S)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)
SODIUM BENZOATE (UNII: OJ245FE5EU)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ADENOSINE (UNII: K72T3FS567)
PEG-8 LAURATE (UNII: 762O8IWA10)
HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV)
POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6)
AMMONIUM ACRYLOYLDIMETHYLTAURATE (UNII: KBC00G95HI)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
XANTHAN GUM (UNII: TTV12P4NEE)
BENZYL ALCOHOL (UNII: LKG8494WBH)
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 ANHYDROUS (UNII: 8NLQ36F6MM)
CETYL ALCOHOL (UNII: 936JST6JCN)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70581-020-04	15 mL in 1 JAR; Type 0: Not a Combination Product	03/10/2022
2	NDC: 70581-020-01	1 in 1 CARTON	03/10/2022
2		30 mL in 1 JAR; Type 0: Not a Combination Product
3	NDC: 70581-020-00	1 in 1 CARTON	03/10/2022
3		5 mL in 1 TUBE; Type 0: Not a Combination Product
4	NDC: 70581-020-02	1 in 1 CARTON	03/10/2022
4		50 mL in 1 JAR; Type 0: Not a Combination Product
5	NDC: 70581-020-03	1 in 1 CARTON	03/10/2022
5		75 mL 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 Drug	M020	03/10/2022

Labeler - BPS 60 (272259304)