FDA.reportPublic FDA data

CITY BLOCK SHEER

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 | PADC 1 | 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
2010-03-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:24:07

Label at a glance#

ProductCITY BLOCK SHEER SPF 25 OIL FREE DAILY FACE PROTECTOR
Active ingredientTITANIUM DIOXIDE, ZINC OXIDE
Label structure3 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS: ZINC OXIDE 7.3%, TITANIUM DIOXIDE 6.9%

WARNINGS SECTION

WARNING: FOR EXTERNAL USE ONLY. KEEP OUT OF EYES. RINSE WITH WATER TO REMOVE. STOP USE AND ASK A DOCTOR IF RASH OR IRRITATION DEVELOPS AND LASTS. KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP RIGHT AWAY.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CLINIQUE CITY BLOCK SHEER SPF 25 OIL FREE FACE PROTECTOR

1.4 FL. OZ./ 40 mL

CLINIQUE LABORATORIES, DISTR.

NY, NY 10022

CLINIQUE.COM


FOLDING CARTONFOLDING CARTON

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49527-989-012020-01-31C16284748780-19d75b9d0-dc4e-f424-e053-dadaa90a57ce7886ad69-754f-4ef0-8a26-f345cb881855

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49527-989-01CITY BLOCK SHEERSPF 25 OIL FREE DAILY FACE PROTECTOR1 in 1 CARTONLOTION11
49527-989-02CITY BLOCK SHEERSPF 25 OIL FREE DAILY FACE PROTECTOR40 mL in 1 TUBELOTION401

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49527-989CITY BLOCK SHEER SPF 25 OIL FREE DAILY FACE PROTECTOR (TITANIUM DIOXIDE, ZINC OXIDE) LOTION [CLINIQUE LABORATORIES INC.]1Legacy NDC, 2 package rows20100401_7886ad69-754f-4ef0-8a26-f345cb881855.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP1
ZINC OXIDEACTIVE INGREDIENTSOI2LOH54Z1
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP1
ZINC OXIDEACTIVE MOIETYSOI2LOH54Z1

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49527-98949527-989-02, 49527-989-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
TITANIUM DIOXIDE15FIX9V2JPACTIB
ZINC OXIDESOI2LOH54ZACTIB

Source Document#

Source XML

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
da7f4dee-33bc-4add-a1ba-821bd8e316447886ad69-754f-4ef0-8a26-f345cb8818552010-03-31WarningsExact identifier
spl id: da7f4dee-33bc-4add-a1ba-821bd8e31644
spl set id: 7886ad69-754f-4ef0-8a26-f345cb881855

Reported adverse events (FAERS/openFDA)#

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