FDA.reportPublic FDA data

Omnilux Mineral Facial Sunscreen

Manufacturer
The Lotus Global Group, Inc, dba GlobalMed Technologies | Nanophase Technologies Corporation
Effective date
2024-08-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:56:40

Label at a glance#

ProductOmnilux Mineral Facial Sunscreen
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

Omnilux Mineral Facial Sunscreen

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

Omnilux Mineral Facial Sunscreen

INACTIVE INGREDIENT SECTION

Inactive ingredientsInactive ingredients

Omnilux Mineral Facial Sunscreen

INDICATIONS & USAGE SECTION

Indications & usageIndications & usage

Omnilux Mineral Facial Sunscreen

OTC - ACTIVE INGREDIENT SECTION

Active IngredientsActive Ingredients

Omnilux Mineral Facial Sunscreen

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of childrenkeep out of reach of children

Omnilux Mineral Facial Sunscreen

OTC - PURPOSE SECTION

purposepurpose

Omnilux Mineral Facial Sunscreen

WARNINGS SECTION

Warning LabelWarning Label

Omnilux Mineral Facial Sunscreen

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83866-6202OMNILUX MINERAL FACIAL SUNSCREEN (ZINC OXIDE) LOTION [THE LOTUS GLOBAL GROUP, INC, DBA GLOBALMED TECHNOLOGIES]1Unmatched20240816_1fab0031-59f8-36cd-e063-6394a90a8aef.zip

Products#

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

DailyMed product names page 1 of 1 · 32 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83866-620283866-6202-1, 83866-6202-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 31 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALLANTOIN344S277G0ZIACT
SODIUM HYDROXIDE55X04QC32IIACT
LECITHIN, SOYBEAN1DI56QDM62IACT
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE9229XJ4V12IACT
HYDROLYZED JOJOBA ESTERS (ACID FORM)UDR641JW8WIACT
METHYLPROPANEDIOLN8F53B3R4RIACT
CAPRYLYL GLYCOL00YIU5438UIACT
PHENYLPROPANOL0F897O3O4MIACT
XANTHAN GUMTTV12P4NEEIACT
ISOAMYL LAURATEM1SLX00M3MIACT
HEXYLENE GLYCOLKEH0A3F75JIACT
TOCOPHEROLR0ZB2556P8IACT
CETYL ALCOHOL936JST6JCNIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
GLYCERINPDC6A3C0OXIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
WATER059QF0KO0RIACT
.ALPHA.-BISABOLOL, (+)-105S6I733ZIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
CETETH-20I835H2IHHXIACT
PULLULAN8ZQ0AYU1TTIACT
SQUALANEGW89575KF9IACT
STEARETH-20L0Q8IK9E08IACT
ZINC OXIDESOI2LOH54ZACTIB
ALOE VERA LEAFZY81Z83H0XIACT
FERRIC OXIDE YELLOWEX438O2MRTIACT
PEG-75 STEARATEOT38R0N74HIACT
TETRASODIUM GLUTAMATE DIACETATE5EHL50I4MYIACT
POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE687U3PEB2YIACT
PHENOXYETHANOLHIE492ZZ3TIACT
RUTIN5G06TVY3R7IACT

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
47e1b275-7274-a3c0-e063-6294a90adb1c1fab0031-59f8-36cd-e063-6394a90a8aef2026-01-08WarningsExact identifier
spl set id: 1fab0031-59f8-36cd-e063-6394a90a8aef

Reported adverse events (FAERS/openFDA)#

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