FDA.reportPublic FDA data

YOUTH SURGE

Manufacturer
CLINIQUE LABORATORIES INC | ESTEE LAUDER N.V. | Len-Ron Manufacturing Division of Aramis Inc. | Aramis Inc. | Northtec Bristol | Northtec Keystone | PADC 1 | Estee Lauder Pennsylvania Distribution Center 2 | Estee Lauder Cosmetics, Ltd. | Estee Lauder Cosmetics, Ltd | Estee Lauder Cosmetics Distribution Center | Estee Lauder Kabushiki Kaisha | Whitman Laboratories Ltd. | Aveda Corporation
Effective date
2010-04-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:24:10

Label at a glance#

ProductYOUTH SURGE SPF 15 AGE DECELERATING MOISTURIZER DRY COMBINATION SKIN
Active ingredientOCTINOXATE, OCTISALATE, TITANIUM DIOXIDE
Label structure3 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS: OCTINOXATE 7.5%, OCTISALATE 3.5%, TITANIUM DIOXIDE, 1.2%

WARNINGS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PRINCIPLE DISPLAY PANEL  1.7 OZ CARTON

CLINIQUE

YOUTH SURGE SPF 15
AGE DECELERATING MOISTURIZER
DRY COMBINATION

NET WT. 1.7 OZ/ 50 ML


CLINIQUE LABORATORIES DISTR.

NEW YORK, NY  10022

6NFC

CLINIQUE.COM


FOLDING CARTONFOLDING CARTON

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49527-730-012019-10-21C16284748780-1956f9ecf-d869-621f-e053-dbdaa90a74ad297d98d1-68d3-444c-aefc-dda749268bdb

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49527-730-01YOUTH SURGE SPF 15 AGE DECELERATING MOISTURIZER DRY COMBINATION SKIN1 in 1 CARTONCREAM11
49527-730-02YOUTH SURGE SPF 15 AGE DECELERATING MOISTURIZER DRY COMBINATION SKIN50 mL in 1 JARCREAM501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49527-730YOUTH SURGE (OCTINOXATE OCTISALATE TITANIUM DIOXIDE ) CREAM [CLINIQUE LABORATORIES INC]1Legacy NDC, 2 package rows20100405_297d98d1-68d3-444c-aefc-dda749268bdb.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
OCTISALATEACTIVE INGREDIENT4X49Y0596W1
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
OCTISALATEACTIVE MOIETY4X49Y0596W1
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP1

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49527-73049527-730-02, 49527-730-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
OCTINOXATE4Y5P7MUD51ACTIB
OCTISALATE4X49Y0596WACTIB
TITANIUM DIOXIDE15FIX9V2JPACTIB

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
5759b0af-ab98-41ce-ac9f-9725d5788e26297d98d1-68d3-444c-aefc-dda749268bdb2010-04-02WarningsExact identifier
spl id: 5759b0af-ab98-41ce-ac9f-9725d5788e26
spl set id: 297d98d1-68d3-444c-aefc-dda749268bdb

Reported adverse events (FAERS/openFDA)#

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