FDA.reportPublic FDA data

MOISTURE SURGE

Manufacturer
CLINIQUE LABORATORIES 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
2011-01-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:26:57

Label at a glance#

ProductMOISTURE SURGE TINTED MOISTURIZER SPF 15
Active ingredientTITANIUM DIOXIDE, OCTISALATE, OCTINOXATE
Label structure5 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

active ingredients: titanium dioxide 6.80% [] octisalate 5.00% [] octinoxate 2.80%

INACTIVE INGREDIENT SECTION

inactive ingredients: water\aqua\eau [] methyl trimethicone [] butylene glycol [] glycerin [] trimethylsiloxysilicate [] peg-10 dimethicone [] octyldodecyl neopentanoate [] lauryl peg-9 polydimethylsiloxyethyl dimethicone [] betula alba (birch) bark extract [] saccharomyces lysate extract [] aloe barbadensis leaf water [] ethylhexylglycerin [] dimethicone [] trehalose [] sorbitol [] sodium hyaluronate [] menthol [] trihydroxystearin [] hydroxyapatite [] tocopheryl acetate [] lecithin [] triethoxycaprylylsilane [] laureth-7 [] magnesium aluminum silicate [] cetrimonium chloride [] pvp [] dimethicone/peg-10/15 crosspolymer [] stearic acid [] aluminum hydroxide [] silica [] sodium chloride [] xanthan gum [] dipropylene glycol [] disodium edta [] sodium citrate [] sodium dehydroacetate [] chlorphenesin [] phenoxyethanol []  [+/- mica [] titanium dioxide (ci 77891) [] zinc oxide (ci 77947) [] iron oxides (ci 77491, ci 77492, ci 77499)

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:

CLINIQUE

MOISTURE SURGE

TINTED MOISTURIZER

SPF 15

1 FL OZ LIQ/ 30 ML

CLINIQUE LABS DIST

NY NY 10022


FOLDING CARTONFOLDING CARTON

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49527-007-012019-10-29C16284748780-1960f7f55-d499-8e05-e053-dbdaa90a074ac9ac427f-6626-435f-aec3-3b90019ee50b

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49527-007-01MOISTURE SURGETINTED MOISTURIZER SPF 151 in 1 CARTONLOTION11
49527-007-02MOISTURE SURGETINTED MOISTURIZER SPF 1530 mL in 1 BOTTLE, PLASTICLOTION301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49527-007MOISTURE SURGE TINTED MOISTURIZER SPF 15 (TITANIUM DIOXIDE, OCTISALATE, OCTINOXATE) LOTION [CLINIQUE LABORATORIES INC]1Legacy NDC, 2 package rows20110118_c9ac427f-6626-435f-aec3-3b90019ee50b.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
OCTISALATEACTIVE INGREDIENT4X49Y0596W1
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
OCTISALATEACTIVE MOIETY4X49Y0596W1
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 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49527-00749527-007-02, 49527-007-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
TITANIUM DIOXIDE15FIX9V2JPACTIB
OCTISALATE4X49Y0596WACTIB
OCTINOXATE4Y5P7MUD51ACTIB
BUTYLENE GLYCOL3XUS85K0RAIACT
WATER059QF0KO0RIACT
DIMETHICONE92RU3N3Y1OIACT

Source Document#

Source XML · Source PDF

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
bdbcc35e-1e60-4bf4-818e-c44dd90e841cc9ac427f-6626-435f-aec3-3b90019ee50b2011-01-14WarningsExact identifier
spl id: bdbcc35e-1e60-4bf4-818e-c44dd90e841c
spl set id: c9ac427f-6626-435f-aec3-3b90019ee50b

Reported adverse events (FAERS/openFDA)#

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