NATURAL FINISH

Manufacturer
Bobbi Brown Professional Cosmetics 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 | J. O. COSMETICS
Effective date
2010-05-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:53:13

Label at a glance#

ProductNATURAL FINISH LONG LASTING FOUNDATION SPF 15
Active ingredientOCTINOXATE, TITANIUM DIOXIDE
Label structure4 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS: OCTINOXATE 7.50% [] TITANIUM DIOXIDE 1.00%

OTC - WHEN USING SECTION

DIRECTIONS: SHAKE WELL BEFORE USE

WARNINGS SECTION


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


PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL:


BOBBI BROWN

NATURAL FINISH

LONG LASTING FOUNDATION SPF 15


1FL OZ./LIQ OZ/30 ML


DIST. BOBBI BROWN PROFESSIONAL COSMETICS INC.
NEW YORK, NY 10022



FOLDING CARTONFOLDING CARTON


FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64141-002-012025-04-22C16284748780-1956f9ecf-d45b-621f-e053-dbdaa90a74ad6d572e5e-c45e-43f5-8a13-5780328dec05
64141-002-012019-10-21C16284748780-1956f9ecf-d45b-621f-e053-dbdaa90a74ad6d572e5e-c45e-43f5-8a13-5780328dec05

DailyMed Socrata Ingredients#

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

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
64141-00264141-002-02, 64141-002-01

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
TITANIUM DIOXIDE15FIX9V2JPACTIB

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
cfdc1255-795e-4ecc-9d5d-52abb8d854266d572e5e-c45e-43f5-8a13-5780328dec052025-04-17WarningsExact identifier
spl set id: 6d572e5e-c45e-43f5-8a13-5780328dec05

Reported adverse events (FAERS/openFDA)#

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