OMNILUX MINERAL FACIAL SUNSCREEN- zinc oxide lotion

Omnilux Mineral Facial Sunscreen by

Drug Labeling and Warnings

Omnilux Mineral Facial Sunscreen by is a Otc medication manufactured, distributed, or labeled by The Lotus Global Group, Inc, dba GlobalMed Technologies, Nanophase Technologies Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Omnilux Mineral Facial Sunscreen

Omnilux Mineral Facial Sunscreen

Omnilux Mineral Facial Sunscreen

Omnilux Mineral Facial Sunscreen

Omnilux Mineral Facial Sunscreen

Omnilux Mineral Facial Sunscreen

Omnilux Mineral Facial Sunscreen

Omnilux Mineral Facial Sunscreen

INGREDIENTS AND APPEARANCE

OMNILUX MINERAL FACIAL SUNSCREEN 
zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83866-6202
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	132 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALLANTOIN (UNII: 344S277G0Z)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)
HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)
METHYLPROPANEDIOL (UNII: N8F53B3R4R)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
PHENYLPROPANOL (UNII: 0F897O3O4M)
XANTHAN GUM (UNII: TTV12P4NEE)
ISOAMYL LAURATE (UNII: M1SLX00M3M)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
TOCOPHEROL (UNII: R0ZB2556P8)
CETYL ALCOHOL (UNII: 936JST6JCN)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
GLYCERIN (UNII: PDC6A3C0OX)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
WATER (UNII: 059QF0KO0R)
.ALPHA.-BISABOLOL, (+)- (UNII: 105S6I733Z)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
CETETH-20 (UNII: I835H2IHHX)
PULLULAN (UNII: 8ZQ0AYU1TT)
SQUALANE (UNII: GW89575KF9)
STEARETH-20 (UNII: L0Q8IK9E08)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
PEG-75 STEARATE (UNII: OT38R0N74H)
TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE (UNII: 687U3PEB2Y)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
RUTIN (UNII: 5G06TVY3R7)

Product Characteristics
Color	yellow	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83866-6202-2	1 in 1 CARTON	07/26/2024
1	NDC: 83866-6202-1	50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	07/26/2024

Labeler - The Lotus Global Group, Inc, dba GlobalMed Technologies (969797406)

Registrant - Nanophase Technologies Corporation (623502044)