FDA.reportPublic FDA data

Mineral Foundation SPF 30-5W

Manufacturer
Allure Labs Inc.
Effective date
2017-12-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:53:29

Label at a glance#

ProductMineral Foundation SPF 30-5W
Active ingredientZINC OXIDE, TITANIUM DIOXIDE
Label structure4 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients:

Zinc Oxide - 5.5%

Titanium Dioxide - 4.4%

INDICATIONS & USAGE SECTION

Direction: Apply with a foundation brush for flawless coverage. Discontinue use if irritation develpos.

DOSAGE & ADMINISTRATION SECTION

Directions: Apply with a foundation brush for flawless coverage. Discontinue use if irritation develops.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Manufactured for DermaQuest Inc.

Hayward, CA 94544

dermaminerals.com

1272 GK, NL

Made in USA

Image MF SPF 30-5WImage MF SPF 30-5W

Image MF SPF 30-5WImage MF SPF 30-5W

Image MF SPF 30-5WImage MF SPF 30-5W

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62742-4099-22023-01-30C16284748780-1f386c64a-431c-0266-e053-dadaa90a7c1aDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62742-4099-1Mineral Foundation SPF 30-5W29.6 mL in 1 TUBECREAM29.61
62742-4099-2Mineral Foundation SPF 30-5W1 in 1 CARTONCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62742-4099MINERAL FOUNDATION SPF 30-5W (ZINC OXIDE AND TITANIUM DIOXIDE) CREAM [ALLURE LABS INC.]1Legacy NDC, 2 package rows20171214_e71e727b-ff38-4620-bbd1-051f77001e16.zip

Products#

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

DailyMed product names page 1 of 1 · 39 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62742-409962742-4099-1, 62742-4099-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 37 matching rows.

Name, UNII, Kind table
NameUNIIKind
ZINC OXIDESOI2LOH54ZACTIB
TITANIUM DIOXIDE15FIX9V2JPACTIB
DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE)UF7620L1W6IACT
DIMETHICONE92RU3N3Y1OIACT
WATER059QF0KO0RIACT
CYCLOMETHICONENMQ347994ZIACT
PEG/PPG-18/18 DIMETHICONE9H0AO7T794IACT
PERFLUNAFENE54A06VV62NIACT
LECITHIN, SOYBEAN1DI56QDM62IACT
SACCHAROMYCES LYSATER85W246Z1CIACT
SODIUM PYRROLIDONE CARBOXYLATE469OTG57A2IACT
PPG-12/SMDI COPOLYMER1BK9DDD24EIACT
MAGNESIUM SILICATE9B9691B2N9IACT
NYLON-12446U8J075BIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
SANDALWOOD3641YW25N2IACT
PHELLODENDRON AMURENSE BARKPBG27B754GIACT
BARLEY5PWM7YLI7RIACT
HYALURONATE SODIUMYSE9PPT4THIACT
GLYCERINPDC6A3C0OXIACT
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%)R33S7TK2EPIACT
ARTEMISIA VULGARIS ROOT32MP823R8SIACT
CENTELLA ASIATICA7M867G6T1UIACT
CETEARYL OLIVATE58B69Q84JOIACT
SORBITAN OLIVATEMDL271E3GRIACT
TETRAHEXYLDECYL ASCORBATE9LBV3F07AZIACT
POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S)RLA2U05Z4QIACT
STEARIC ACID4ELV7Z65APIACT
ALUMINUM HYDROXIDE5QB0T2IUN0IACT
POLYGLYCERYL-4 ISOSTEARATE820DPX33S7IACT
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2)V2W71V8T0XIACT
HEXYL LAURATE4CG9F9W01QIACT
PHENOXYETHANOLHIE492ZZ3TIACT
CAPRYLYL GLYCOL00YIU5438UIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
HEXYLENE GLYCOLKEH0A3F75JIACT
ALOE VERA LEAFZY81Z83H0XIACT

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
2105dd07-3944-4eae-a33f-465460cc8688e71e727b-ff38-4620-bbd1-051f77001e162017-12-05Exact identifier
spl id: 2105dd07-3944-4eae-a33f-465460cc8688
spl set id: e71e727b-ff38-4620-bbd1-051f77001e16

Reported adverse events (FAERS/openFDA)#

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