CATHYCAT ESSENCE SUN BB- titanium dioxide, octinoxate, zinc oxide, amiloxate liquid

CATHYCAT ESSENCE SUN BB by

Drug Labeling and Warnings

CATHYCAT ESSENCE SUN BB by is a Otc medication manufactured, distributed, or labeled by LG Household and Healthcare, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Titanium Dioxide 13.76%

OCTINOXATE 7%

Zinc Oxide 3.92%

AMILOXATE 1%

WARNINGS AND PRECAUTIONS

For external use only.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. Is swallowed, get medical help or contact a Poison Control Center right away.

WHEN USING

Keep out of eyes. Rinse with water to remove.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CATHYCAT ESSENCE SUN BB 
titanium dioxide, octinoxate, zinc oxide, amiloxate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53208-528
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Titanium Dioxide (UNII: 15FIX9V2JP) (Titanium Dioxide - UNII:15FIX9V2JP)	Titanium Dioxide	13.76176 mL  in 100 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	7 mL  in 100 mL
Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z)	Zinc Oxide	3.92 mL  in 100 mL
AMILOXATE (UNII: 376KTP06K8) (AMILOXATE - UNII:376KTP06K8)	AMILOXATE	1 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
Dipropylene Glycol (UNII: E107L85C40)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
Dicaprylyl Carbonate (UNII: 609A3V1SUA)
Sodium Chloride (UNII: 451W47IQ8X)
METHYL METHACRYLATE (UNII: 196OC77688)
Glycerin (UNII: PDC6A3C0OX)
POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
Sorbitan (UNII: 6O92ICV9RU)
Hectorite (UNII: 08X4KI73EZ)
Dimethicone (UNII: 92RU3N3Y1O)
Aluminum Hydroxide (UNII: 5QB0T2IUN0)
Stearic Acid (UNII: 4ELV7Z65AP)
Trihydroxystearin (UNII: 06YD7896S3)
Methylparaben (UNII: A2I8C7HI9T)
CHLORPHENESIN (UNII: I670DAL4SZ)
Triethoxycaprylylsilane (UNII: LDC331P08E)
Propylparaben (UNII: Z8IX2SC1OH)
Iron (UNII: E1UOL152H7)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
EDETATE DISODIUM (UNII: 7FLD91C86K)
Butylphenyl Methylpropional (UNII: T7540GJV69)
Butylene Glycol (UNII: 3XUS85K0RA)
FERRIC OXIDE RED (UNII: 1K09F3G675)
LINALOOL, DL- (UNII: D81QY6I88E)
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
Phenoxyethanol (UNII: HIE492ZZ3T)
Butylparaben (UNII: 3QPI1U3FV8)
Ethylparaben (UNII: 14255EXE39)
Isobutylparaben (UNII: 0QQJ25X58G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53208-528-02	1 in 1 BOX
1	NDC: 53208-528-01	50 mL in 1 CONTAINER

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	04/15/2011

Labeler - LG Household and Healthcare, Inc. (688276187)

Registrant - LG Household and Healthcare, Inc. (688276187)

Establishment
Name	Address	ID/FEI	Business Operations
LG Household and Healthcare, Inc.		688276187	manufacture