MINERALIZE FOUNDATION

Manufacturer
MAKE-UP ART COSMETICS | 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. | INTERCOS
Effective date
2010-05-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:25:20

Label at a glance#

ProductMINERALIZE FOUNDATION SPF 15
Active ingredientOCTINOXATE
Label structure3 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENT: OCTINOXATE 2.5%

WARNINGS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL:

MAC

MINERALIZE

SPF 15 FOUNDATION


NET WT./POIDS NET 10g/0.35 US OZ

DIST. BY MAKE-UP ART COSMETICS

TORONTO, ONTARIO, CANADA M5V 1R7

FOLDING CARTONFOLDING CARTON

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
40046-0037-12019-10-21C16284748780-1956f9ecf-d1e5-621f-e053-dbdaa90a74ad922394f8-e3c7-405f-905c-4195145c46aa

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
40046-0037-1MINERALIZE FOUNDATIONSPF 151 in 1 CARTONCREAM11
40046-0037-2MINERALIZE FOUNDATIONSPF 1510 g in 1 JARCREAM101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
40046-0037MINERALIZE FOUNDATION SPF 15 (OCTINOXATE) CREAM [MAKE-UP ART COSMETICS]1Legacy NDC, 2 package rows20100728_922394f8-e3c7-405f-905c-4195145c46aa.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
OCTINOXATEACTIVE MOIETY4Y5P7MUD511

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
40046-003740046-0037-2, 40046-0037-1

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
OCTINOXATE4Y5P7MUD51ACTIB

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
db752197-9555-43ce-adc3-7fb0b7194f2c922394f8-e3c7-405f-905c-4195145c46aa2010-05-18WarningsExact identifier
spl id: db752197-9555-43ce-adc3-7fb0b7194f2c
spl set id: 922394f8-e3c7-405f-905c-4195145c46aa

Reported adverse events (FAERS/openFDA)#

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