ESTEE LAUDER MULTI-DEFENSE AQUA UV gel BROAD SPECTRUM SPF 50

Manufacturer
ESTEE LAUDER INC | Estee Lauder Companies Inc. | Estee Lauder N.V.
Effective date
2024-12-25
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
full-release
Hydrated at
2026-06-01 00:48:45

Label at a glance#

ProductESTEE LAUDER MULTI-DEFENSE AQUA UV gel BROAD SPECTRUM SPF 50
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE
Label structure8 sections

Indications and 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

Dosage and administration

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: li...

Storage and handling

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

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active ingredientsPurpose
Avobenzone 3.0%Sunscreen
Homosalate 5.0%Sunscreen
Octisalate 4.5%Sunscreen
Octocrylene 2.8%Sunscreen
Oxybenzone 3.0%Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • 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

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin

OTC - WHEN USING SECTION

When using this product keep out of eyes. Rinse with water to remove.

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

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

INACTIVE INGREDIENT SECTION

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

STORAGE AND HANDLING SECTION

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

PRINCIPAL DISPLAY PANEL - 30 ml Tube Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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
PRINCIPAL DISPLAY PANEL - 30 ml Tube Carton

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11559-060-01ESTEE LAUDER MULTI-DEFENSE AQUA UV gel BROAD SPECTRUM SPF 5030 mL in 1 TUBELOTION3010
11559-060-01ESTEE LAUDER MULTI-DEFENSE AQUA UV gel BROAD SPECTRUM SPF 501 in 1 CARTONLOTION110

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11559-060ESTEE LAUDER MULTI-DEFENSE AQUA UV GEL BROAD SPECTRUM SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, AND OXYBENZONE) LOTION [ESTEE LAUDER INC]10Current NDC, Legacy NDC, 2 package rows20241227_0770e251-95d0-43de-88f1-bc0a29811e4e.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 2 · 52 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11559-06011559-060-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 2 · 50 matching rows.

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ESTEE LAUDER MULTI-DEFENSE AQUA UV gel BROAD SPECTRUM SPF 50AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, AND OXYBENZONEESTEE LAUDER INC0770e251-95d0-43de-88f1-bc0a29811e4e2024-12-25WarningsExact identifier
ndc (package): 11559-060-01
ndc (product): 11559-060
ndc11 (package): 11559006001
spl id: 2a15b78c-0356-b0b0-e063-6294a90a09db
spl set id: 0770e251-95d0-43de-88f1-bc0a29811e4e

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.