Label: CX DAILY EYE PROTECTOR SPF 15- titanium dioxide gel
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Contains inactivated NDC Code(s)
NDC Code(s): 49527-750-01, 49527-750-02 - Packager: CLINIQUE LABORATORIES 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 September 13, 2011
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- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
inactive ingredients: cyclopentasiloxane [] dimethicone [] trioctyldodecyl citrate [] silica [] isododecane [] vinyl dimethicone/methicone silsesquioxane crosspolymer [] dimethicone/vinyl dimethicone crosspolymer [] trimethylsiloxysilicate [] polysilicone-11 [] aluminum stearate [] mimosa tenuiflora bark extract [] tocopheryl acetate [] vitis vinifera (grape) seed oil [] 7-dehydrocholesterol [] tricaprylin [] tetrahexyldecyl ascorbate [] butylene glycol [] water\aqua\eau [] tocotrienols [] aminopropyl ascorbyl phosphate [] stearic acid [] methicone [] phenoxyethanol [] mica [] iron oxides (ci 77491, ci 77492, ci 77499) [] titanium dioxide (ci 77891)
- WARNINGS
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INGREDIENTS AND APPEARANCE
CX DAILY EYE PROTECTOR SPF 15
titanium dioxide gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49527-750 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 7.8 mL in 100 mL Inactive Ingredients Ingredient Name Strength CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) DIMETHICONE (UNII: 92RU3N3Y1O) TRICAPRYLYL CITRATE (UNII: BXW1GAI4TA) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) ISODODECANE (UNII: A8289P68Y2) ALUMINUM STEARATE (UNII: U6XF9NP8HM) MIMOSA TENUIFLORA BARK (UNII: 515MQE449I) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) GRAPE SEED OIL (UNII: 930MLC8XGG) 7-DEHYDROCHOLESTEROL (UNII: BK1IU07GKF) TRICAPRYLIN (UNII: 6P92858988) TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) WATER (UNII: 059QF0KO0R) STEARIC ACID (UNII: 4ELV7Z65AP) PHENOXYETHANOL (UNII: HIE492ZZ3T) MICA (UNII: V8A1AW0880) FERRIC OXIDE RED (UNII: 1K09F3G675) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49527-750-01 1 in 1 CARTON 1 NDC:49527-750-02 7 mL in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 02/01/2002 Labeler - CLINIQUE LABORATORIES INC (173047747) Establishment Name Address ID/FEI Business Operations ESTEE LAUDER COSMETICS, LTD 205952385 manufacture Establishment Name Address ID/FEI Business Operations ESTEE LAUDER N.V. 370151326 manufacture Establishment Name Address ID/FEI Business Operations Len-Ron Manufacturing Division of Aramis Inc. 809771152 manufacture Establishment Name Address ID/FEI Business Operations Aramis Inc. 042918826 manufacture Establishment Name Address ID/FEI Business Operations Northtec Bristol 949264774 manufacture, relabel, repack Establishment Name Address ID/FEI Business Operations Northtec Keystone 618107429 manufacture, relabel, repack Establishment Name Address ID/FEI Business Operations Estee Lauder Pennsylvania Distribution Center 2 828534516 manufacture, relabel, repack Establishment Name Address ID/FEI Business Operations Estee Lauder Cosmetics, Ltd. 255175580 manufacture Establishment Name Address ID/FEI Business Operations Estee Lauder Cosmetics, Ltd 253616536 manufacture Establishment Name Address ID/FEI Business Operations Estee Lauder Cosmetics Distribution Center 208579636 repack, relabel Establishment Name Address ID/FEI Business Operations Estee Lauder Kabushiki Kaisha 712808195 relabel, repack Establishment Name Address ID/FEI Business Operations Whitman Laboratories Ltd. 216866277 manufacture Establishment Name Address ID/FEI Business Operations Aveda Corporation 071352058 manufacture
