FDA.reportPublic FDA data

RENUTRIV

Manufacturer
ESTEE LAUDER INC | ESTEE LAUDER COSMETICS, LTD | ESTEE LAUDER N.V. | Len-Ron Manufacturing Division of Aramis Inc. | Aramis Inc. | Northtec Bristol | Northtec Keystone | Estee Lauder Pennsylvania Distribution Center 2 | Estee Lauder Cosmetics, Ltd. | Estee Lauder Cosmetics Distribution Center | Estee Lauder Kabushiki Kaisha | Whitman Laboratories Ltd. | Aveda Corporation
Effective date
2010-12-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:26:30

Label at a glance#

ProductRENUTRIV ULTIMATE RADIANCE MAKEUP SPF 15
Active ingredientOCTINOXATE, TITANIUM DIOXIDE
Label structure5 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS: OCTINOXATE 2.20% [] TITANIUM DIOXIDE 1.40%

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: WATER\AQUA\EAU [] CYCLOPENTASILOXANE [] PHENYL TRIMETHICONE [] BUTYLENE GLYCOL [] DIMETHICONE [] ISOCETYL ALCOHOL [] CAPRYLIC/CAPRIC TRIGLYCERIDE [] ISOHEXADECANE [] WHEAT GERM GLYCERIDES [] PEG/PPG-20/20 DIMETHICONE [] SORBITAN SESQUIOLEATE [] MAGNESIUM SULFATE [] TRIBEHENIN [] HYDROLYZED WHEAT PROTEIN [] POLYSILICONE-11 [] RUBY POWDER [] SAPPHIRE POWDER [] NEPHRITE POWDER [] ETHYLHEXYLGLYCERIN [] PEARL POWDER [] LAURETH-7 [] METHICONE [] SORBITAN STEARATE [] CHOLESTEROL [] HYDROGENATED LECITHIN [] SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL [] TRIETHYL CITRATE [] LINOLEIC ACID [] DISTEARDIMONIUM HECTORITE [] ETHYLHEXYL PALMITATE [] POLYMETHYLSILSESQUIOXANE [] PROPYLENE CARBONATE [] SODIUM HYALURONATE [] GOLD [] AMETHYST [] BORON NITRIDE [] TRIETHOXYCAPRYLYLSILANE [] ALUMINA [] SORBITAN ISOSTEARATE [] PALMITOYL OLIGOPEPTIDE [] PENTAERYTHRITYL TETRA-DI-T-BUTYL HYDROXYHYDROCINNAMATE [] CETYL PEG/PPG-10/1 DIMETHICONE [] XANTHAN GUM [] ASCORBYL PALMITATE [] TOCOPHERYL ACETATE [] CHLOROXYLENOL [] PHENOXYETHANOL []  [+/- TITANIUM DIOXIDE (CI 77891) [] IRON OXIDES (CI 77491, CI 77492, CI 77499) [] MICA

WARNINGS SECTION

WARNING: KEEP OUT OF EYES. STOP USE IF IRRITATION OCCURS.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL


ESTEE LAUDER

RE-NUTRIV

ULTIMATE RADIANCE MAKEUP

SPF 15


1 FL OZ LIQUID/30 ML


ESTEE LAUDER DISTR.

NY, NY 10022

FOLDING CARTONFOLDING CARTON

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11559-746-012020-01-31C16284748780-19d75b9d0-b0f5-f424-e053-dadaa90a57ce3bd1deb4-fbcb-497e-b3a4-a4e0a8864514

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11559-746-01RENUTRIVULTIMATE RADIANCE MAKEUP SPF 151 in 1 CARTONLIQUID11
11559-746-02RENUTRIVULTIMATE RADIANCE MAKEUP SPF 1530 mL in 1 BOTTLELIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11559-746RENUTRIV ULTIMATE RADIANCE MAKEUP SPF 15 (OCTINOXATE, TITANIUM DIOXIDE) LIQUID [ESTEE LAUDER INC]1Legacy NDC, 2 package rows20101206_3bd1deb4-fbcb-497e-b3a4-a4e0a8864514.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP1
BUTYLENE GLYCOLINACTIVE INGREDIENT3XUS85K0RA1
DIMETHICONEINACTIVE INGREDIENT92RU3N3Y1O1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11559-74611559-746-02, 11559-746-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
OCTINOXATE4Y5P7MUD51ACTIB
TITANIUM DIOXIDE15FIX9V2JPACTIB
WATER059QF0KO0RIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
DIMETHICONE92RU3N3Y1OIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
BUTYLENE GLYCOLBUTYLENE GLYCOL3XUS85K0RASYSTEM / TOPICAL1400 mgExact identifier — unii candidate
2 equally ranked IID candidates
BUTYLENE GLYCOLBUTYLENE GLYCOL3XUS85K0RASYSTEM / TRANSDERMAL8.12 mgExact identifier — unii candidate
2 equally ranked IID candidates

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
8a53c88e-f816-48da-b647-13b847afe0fe3bd1deb4-fbcb-497e-b3a4-a4e0a88645142010-12-02WarningsExact identifier
spl id: 8a53c88e-f816-48da-b647-13b847afe0fe
spl set id: 3bd1deb4-fbcb-497e-b3a4-a4e0a8864514

Reported adverse events (FAERS/openFDA)#

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