ILIA SUPER SERUM SKIN TINT (ST12 KOKKINI)- zinc oxide lotion

ILIA SUPER SERUM SKIN TINT (ST12 KOKKINI) by

Drug Labeling and Warnings

ILIA SUPER SERUM SKIN TINT (ST12 KOKKINI) by is a Otc medication manufactured, distributed, or labeled by Ilia, Inc., Nanophase Technologies Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ILIA SUPER SERUM SKIN TINT (ST12 KOKKINI)

ILIA SUPER SERUM SKIN TINT (ST12 KOKKINI)

ILIA SUPER SERUM SKIN TINT (ST12 KOKKINI)

ILIA SUPER SERUM SKIN TINT (ST12 KOKKINI)

ILIA SUPER SERUM SKIN TINT (ST12 KOKKINI)

ILIA SUPER SERUM SKIN TINT (ST12 KOKKINI)

ILIA SUPER SERUM SKIN TINT (ST12 KOKKINI)

ILIA ST12

INGREDIENTS AND APPEARANCE

ILIA SUPER SERUM SKIN TINT (ST12 KOKKINI) 
zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81110-760
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
SHEA BUTTER (UNII: K49155WL9Y)
ISOAMYL LAURATE (UNII: M1SLX00M3M)
POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
ISOPROPYL ISOSTEARATE (UNII: C67IXB9Y7T)
.ALPHA.-BISABOLOL, (+)- (UNII: 105S6I733Z)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ALLANTOIN (UNII: 344S277G0Z)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
SQUALANE (UNII: GW89575KF9)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
SODIUM MYRISTOYL GLUTAMATE (UNII: AYU7QD893W)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
WATER (UNII: 059QF0KO0R)
NIACINAMIDE (UNII: 25X51I8RD4)
PROPANEDIOL (UNII: 5965N8W85T)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
PHENYLPROPANOL (UNII: 0F897O3O4M)
METHYLPROPANEDIOL (UNII: N8F53B3R4R)

Product Characteristics
Color	brown	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81110-760-02	1 in 1 CARTON	01/20/2020
1	NDC: 81110-760-01	30 mL in 1 BOTTLE, DROPPER; 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	01/20/2020

Labeler - Ilia, Inc. (078503090)

Registrant - Nanophase Technologies Corporation (623502044)

Establishment
Name	Address	ID/FEI	Business Operations
Nanophase Technologies Corporation		050383046	api manufacture(81110-760)

Establishment
Name	Address	ID/FEI	Business Operations
Nanophase Technologies Corporation		118812921	pack(81110-760) , manufacture(81110-760)

Establishment
Name	Address	ID/FEI	Business Operations
Nanophase Technologies Corporation		623502044	manufacture(81110-760) , api manufacture(81110-760)