FDA.reportPublic FDA data

LONG LAST GLOSSWEAR

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
2010-04-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:24:15

Label at a glance#

ProductLONG LAST GLOSSWEAR SPF 15
Active ingredientOCTINOXATE, OCTISALATE
Label structure3 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

active ingredients: octinoxate 7.50% [] octisalate 4.00%

WARNINGS SECTION

warning: stop use if irritation occurs

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL:

CLINIQUE
LONG LAST GLOSSWEAR SPF 15

0.20 FL OZ LIQ/6 ML



CLINIQUE LABORATORIES DIST.
NEW YORK, NY 10022

WWW.CLINIQUE.COM

6LH0
FOLDING CARTON
FOLDING CARTON

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49527-743-012019-10-21C16284748780-1956f9ecf-cebb-621f-e053-dbdaa90a74adfd8bfd97-2628-4c4e-82fb-a88c2b22f6ff

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49527-743-01LONG LAST GLOSSWEARSPF 151 in 1 CARTONLIQUID11
49527-743-02LONG LAST GLOSSWEARSPF 156 mL in 1 TUBE, WITH APPLICATORLIQUID61

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49527-743LONG LAST GLOSSWEAR SPF 15 (OCTINOXATE, OCTISALATE) LIQUID [CLINIQUE LABORATORIES INC]1Legacy NDC, 2 package rows20100417_fd8bfd97-2628-4c4e-82fb-a88c2b22f6ff.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
OCTISALATEACTIVE INGREDIENT4X49Y0596W1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
OCTISALATEACTIVE MOIETY4X49Y0596W1

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
49527-74349527-743-02, 49527-743-01

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
OCTINOXATE4Y5P7MUD51ACTIB
OCTISALATE4X49Y0596WACTIB

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
cf9c4903-54d0-44ad-90a3-f61b6e78cbb2fd8bfd97-2628-4c4e-82fb-a88c2b22f6ff2010-04-05WarningsExact identifier
spl id: cf9c4903-54d0-44ad-90a3-f61b6e78cbb2
spl set id: fd8bfd97-2628-4c4e-82fb-a88c2b22f6ff

Reported adverse events (FAERS/openFDA)#

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