Label: CATHYCAT ESSENCE SUN BB- titanium dioxide, octinoxate, zinc oxide, amiloxate liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 53208-528-01, 53208-528-02 - Packager: LG Household and Healthcare, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated May 16, 2012
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INGREDIENTS AND APPEARANCE
CATHYCAT ESSENCE SUN BB
titanium dioxide, octinoxate, zinc oxide, amiloxate liquidProduct 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
