ESTEE LAUDER MULTI-DEFENSE AQUA UV GEL BROAD SPECTRUM SPF 50- avobenzone, homosalate, octisalate, octocrylene, and oxybenzone lotion 
ESTEE LAUDER 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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ESTĒE LAUDER MULTI-DEFENSE AQUA UV GEL BROAD SPECTRUM SPF 50

Drug Facts

Active ingredientsPurpose
Avobenzone 3.0%Sunscreen
Homosalate 5.0%Sunscreen
Octisalate 4.5%Sunscreen
Octocrylene 2.8%Sunscreen
Oxybenzone 3.0%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 product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

For sunscreen use:

  • apply liberally and evenly 15 minutes before sun exposure
  • reapply at least every two 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

Inactive ingredients

water\aqua\eau • alcohol denat. • butylene glycol • tocopheryl acetate • sodium hyaluronate • camellia sinensis (green tea) leaf extract • anthemis nobilis (chamomile) flower extract • algae extract • triticum vulgare (wheat) germ extract • laminaria ochroleuca extract • polygonum cuspidatum root extract • squalane • hordeum vulgare (barley) extract\extrait d'orge • lilium tigrinum extract • opuntia tuna extract • caffeine • acrylates copolymer • caprylic/capric triglyceride • caprylyl glycol • cholesterol • ergothioneine • glycerin • sucrose • alcaligenes polysaccharides • thermus thermophillus ferment • sorbitan sesquiisostearate • tetrahexyldecyl ascorbate • hexylene glycol • acrylates/ beheneth-25 methacrylate copolymer • sodium hydroxide • dehydroxanthan gum • dipropylene glycol • carbomer • ppg-8-ceteth-20 • dextrin palmitate • cyclodextrin • acrylates/c10-30 alkyl acrylate crosspolymer • sorbeth-30 tetraisostearate • glyceryl stearate • polymethylsilsesquioxane • ammonium acryloyldimethyltaurate/vp copolymer • bht • ethylbisiminomethylguaiacol manganese chloride • disodium edta • phenoxyethanol
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Other information

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

PRINCIPAL DISPLAY PANEL - 30 ml Tube Carton

ESTĒE LAUDER

Perfectionist Pro
Multi-Defense Aqua UV Gel
Broad Spectrum SPF 50
8 Anti-Oxidants

All Skintypes

1 FL. OZ. LIQ./30 ml e

PRINCIPAL DISPLAY PANEL - 30 ml Tube Carton
ESTEE LAUDER MULTI-DEFENSE AQUA UV GEL BROAD SPECTRUM SPF 50 
avobenzone, homosalate, octisalate, octocrylene, and oxybenzone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11559-060
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) OCTISALATE45 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE28 mg  in 1 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE30 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
1,2-BUTANEDIOL (UNII: RUN0H01QEU)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)  
SARGASSUM FILIPENDULA (UNII: 55P66J5H7N)  
WHEAT GERM (UNII: YR3G369F5A)  
LAMINARIA OCHROLEUCA (UNII: 4R2124HE76)  
REYNOUTRIA JAPONICA ROOT (UNII: 7TRV45YZF7)  
SQUALANE (UNII: GW89575KF9)  
HORDEUM VULGARE ROOT (UNII: 790S39483Z)  
LILIUM LANCIFOLIUM BULB (UNII: 47Z05W73EZ)  
OPUNTIA TUNA WHOLE (UNII: DI94T5T0ZY)  
CAFFEINE (UNII: 3G6A5W338E)  
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
CHOLESTEROL (UNII: 97C5T2UQ7J)  
ERGOTHIONEINE (UNII: BDZ3DQM98W)  
GLYCERIN (UNII: PDC6A3C0OX)  
SUCROSE (UNII: C151H8M554)  
ALCALIGENES FAECALIS (UNII: 05KB30NGW2)  
THERMUS THERMOPHILUS LYSATE (UNII: 775R692494)  
SORBITAN SESQUIISOSTEARATE (UNII: VU97D01BF9)  
TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)  
HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
BEHENETH-25 METHACRYLATE (UNII: 108R05PWG6)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
DEHYDROXANTHAN GUM (UNII: 63ZP7I1BQO)  
DIPROPYLENE GLYCOL (UNII: E107L85C40)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
PPG-2-CETETH-9 (UNII: 1OTA54V264)  
DEXTRIN PALMITATE (CORN; 20000 MW) (UNII: 89B2BSF9I3)  
BETADEX (UNII: JV039JZZ3A)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
PEG-10 SORBITAN LAURATE (UNII: 4Z93U4C2WN)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)  
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
ETHYLBISIMINOMETHYLGUAIACOL MANGANESE CHLORIDE (UNII: SM5YJ88LTU)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11559-060-011 in 1 CARTON05/08/2020
130 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart35205/04/2020
Labeler - ESTEE LAUDER INC (005914387)
Registrant - Estee Lauder Companies Inc. (790802086)
Establishment
NameAddressID/FEIBusiness Operations
Whitman Laboratories Ltd.216866277MANUFACTURE(11559-060) , REPACK(11559-060) , RELABEL(11559-060)
Establishment
NameAddressID/FEIBusiness Operations
ESTEE LAUDER COMPANY, THE828534516REPACK(11559-060) , RELABEL(11559-060)
Establishment
NameAddressID/FEIBusiness Operations
Estee Lauder Cosmetics Ltd.202952982MANUFACTURE(11559-060) , REPACK(11559-060) , RELABEL(11559-060)
Establishment
NameAddressID/FEIBusiness Operations
Estee Lauder Cosmetics Ltd.204132062REPACK(11559-060) , RELABEL(11559-060)
Establishment
NameAddressID/FEIBusiness Operations
Estee Lauder N.V.370151326MANUFACTURE(11559-060) , REPACK(11559-060) , RELABEL(11559-060)
Establishment
NameAddressID/FEIBusiness Operations
NORTHTEC INC943871157REPACK(11559-060) , RELABEL(11559-060)
Establishment
NameAddressID/FEIBusiness Operations
NORTHTEC PALC102631997REPACK(11559-060) , RELABEL(11559-060)
Establishment
NameAddressID/FEIBusiness Operations
Len-Ron Manufacturing Division of Aramis Inc.809771152MANUFACTURE(11559-060) , REPACK(11559-060) , RELABEL(11559-060)
Establishment
NameAddressID/FEIBusiness Operations
PADC 1949264774REPACK(11559-060) , RELABEL(11559-060)

Revised: 7/2021
 
ESTEE LAUDER INC