KINLO GOLDEN RAYS SUNSCREEN (MEDIUM TINTED)- zinc oxide lotion

KINLO Golden Rays Sunscreen (Medium Tinted) by

Drug Labeling and Warnings

KINLO Golden Rays Sunscreen (Medium Tinted) by is a Otc medication manufactured, distributed, or labeled by A-Frame SunCo Inc, Nanophase Technologies Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

KINLO Golden Rays Sunscreen (Medium Tinted)

KINLO Golden Rays Sunscreen (Medium Tinted)

KINLO Golden Rays Sunscreen (Medium Tinted)

KINLO Golden Rays Sunscreen (Medium Tinted)

KINLO Golden Rays Sunscreen (Medium Tinted)

KINLO Golden Rays Sunscreen (Medium Tinted)

KINLO Golden Rays Sunscreen (Medium Tinted)

KINLO Golden Rays Sunscreen (Medium Tinted)

INGREDIENTS AND APPEARANCE

KINLO GOLDEN RAYS SUNSCREEN (MEDIUM TINTED) 
zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82184-1173
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)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
DIMETHICONE (UNII: 92RU3N3Y1O)
TRILAURETH-4 PHOSPHATE (UNII: M96W2OLL2V)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
ISODODECANE (UNII: A8289P68Y2)
.ALPHA.-BISABOLOL, (+)- (UNII: 105S6I733Z)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
WATER (UNII: 059QF0KO0R)
NIACINAMIDE (UNII: 25X51I8RD4)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
DIMETHICONOL/PROPYLSILSESQUIOXANE/SILICATE CROSSPOLYMER (450000000 MW) (UNII: 9KB5R958PB)
PROPANEDIOL (UNII: 5965N8W85T)
TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)

Product Characteristics
Color	brown	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82184-1173-2	1 in 1 CARTON	03/08/2022
1	NDC: 82184-1173-1	28 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	03/08/2022

Labeler - A-Frame SunCo Inc (118248026)

Registrant - Nanophase Technologies Corporation (623502044)

Establishment
Name	Address	ID/FEI	Business Operations
Nanophase Technologies Corporation		050383046	api manufacture(82184-1173)

Establishment
Name	Address	ID/FEI	Business Operations
Nanophase Technologies Corporation		623502044	api manufacture(82184-1173) , manufacture(82184-1173) , pack(82184-1173)