Label: RITE AID DAILY MOISTURIZER SPF 15- avobenzone lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 11822-6010-0, 11822-6010-4 - Packager: Rite Aid Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 August 4, 2010
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
- Purpose
- WARNINGS
- OTHER INFORMATION
- USES
- DIRECTIONS
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INACTIVE INGREDIENTS
ARACHIDYL ALCOHOL, ARACHIDYL GLUCOSIDE, BEHENYL ALCOHOL, BENZALKONIUM CHLORIDE, BENZYL ALCOHOL, BHT, BIS-PHENYLPROPYL DIMETHICONE, BUTYLPARABEN, C12-15 ALKYL BENZOATE, C13-14 ISOPARAFFIN, CETEARYL ALCOHOL, CETEARYL GLUCOSIDE, DIMETHICONE, DISODIUM EDTA, ETHYLENE/ACRYLIC COPOLYMER, ETHYLPARABEN, FRAGRANCE, GLYCERINE SOJA (SOYBEAN) SEED EXTRACT, IODOPROPYNYL BUTYLCARBAMATE, ISOBUTYLPARABEN, LAURETH-7, METHYLPARABEN, MICA, PANTHENOL, PHENOXYETHANOL, POLYACRYLAMIDE, POLYMETHYL METHACRYLATE, PROPYLPARABEN, SILICA, STEARETH-2, STEARETH-21, TITANIUM DIOXIDE, WATER, SODIUM HYDROXIDE, CITRIC ACID
- PACKAGE LABEL AND CARTON
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INGREDIENTS AND APPEARANCE
RITE AID DAILY MOISTURIZER SPF 15
avobenzone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-6010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3 mL in 100 mL OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 7.5 mL in 100 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 2 mL in 100 mL Inactive Ingredients Ingredient Name Strength ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU) DOCOSANOL (UNII: 9G1OE216XY) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) BENZYL ALCOHOL (UNII: LKG8494WBH) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) BUTYLPARABEN (UNII: 3QPI1U3FV8) C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) DIMETHICONE (UNII: 92RU3N3Y1O) EDETATE DISODIUM (UNII: 7FLD91C86K) ETHYLPARABEN (UNII: 14255EXE39) GLYCERIN (UNII: PDC6A3C0OX) SOYBEAN (UNII: L7HT8F1ZOD) ISOBUTYLPARABEN (UNII: 0QQJ25X58G) LAURETH-7 (UNII: Z95S6G8201) METHYLPARABEN (UNII: A2I8C7HI9T) MICA (UNII: V8A1AW0880) PANTHENOL (UNII: WV9CM0O67Z) PHENOXYETHANOL (UNII: HIE492ZZ3T) PROPYLPARABEN (UNII: Z8IX2SC1OH) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) LAURETH-2 (UNII: D4D38LT1L5) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) WATER (UNII: 059QF0KO0R) SODIUM HYDROXIDE (UNII: 55X04QC32I) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-6010-4 1 in 1 CARTON 1 NDC:11822-6010-0 118 mL in 1 BOTTLE, PUMP Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 08/04/2010 Labeler - Rite Aid Corporation (014578892)
