CONJU PRINCESS UV SUN BLOCK- ethylhexyl methoxycinnamate cream

Conju Princess UV Sun Block by

Drug Labeling and Warnings

Conju Princess UV Sun Block by is a Otc medication manufactured, distributed, or labeled by Conju Inc, Costree Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

active ingredients: Ethylhexyl methoxycinnamate, 4-methylbenzylidene camphor, butyl methoxydibenzoylmethane, titanium dioxide, zinc oxide

INACTIVE INGREDIENT

inactive ingredient: water, cyclopentasiloxane, dipropylene glycol, glycerin, dimethicone, hexyl laurate, sorbitan olivate, sorbitan sesquioleate, magnesium sulfate, stearic acid, hectorite, aluminum hydroxide, phenoxyethanol, propylparaben, methylparaben, disodium EDTA, fragrance

PURPOSE

Recommended for sensitive skin that needs virtually total sunblock protection

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

Apply daily, with or without make-up to exposed areas

WARNINGS

Avoid eye area. If contact occurs, rinse eyes thoroughly with water.
If  following abnormal symptoms (red specks, swelling, itching) occurs after use, stop use and ask doctor.

DOSAGE & ADMINISTRATION

Apply daily, with or without make-up to exposed areas

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CONJU PRINCESS UV SUN BLOCK 
ethylhexyl methoxycinnamate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59915-4001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	0.075 mL  in 1 mL
ENZACAMENE (UNII: 8I3XWY40L9) (ENZACAMENE - UNII:8I3XWY40L9)	ENZACAMENE	0.05 mL  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	0.0249 mL  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	0.03 mL  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.01 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
GLYCERIN (UNII: PDC6A3C0OX)
DIMETHICONE (UNII: 92RU3N3Y1O)
HEXYL LAURATE (UNII: 4CG9F9W01Q)
SORBITAN OLIVATE (UNII: MDL271E3GR)
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
STEARIC ACID (UNII: 4ELV7Z65AP)
HECTORITE (UNII: 08X4KI73EZ)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
METHYLPARABEN (UNII: A2I8C7HI9T)
EDETATE DISODIUM (UNII: 7FLD91C86K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59915-4001-1	1 mL in 1 POUCH

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		12/18/2010

Labeler - Conju Inc (012345486)

Registrant - Conju Inc (012345486)

Establishment
Name	Address	ID/FEI	Business Operations
Costree Co., Ltd		690345835	manufacture