RITE AID DAILY MOISTURIZER SPF 15- avobenzone lotion

RITE AID DAILY MOISTURIZER by

Drug Labeling and Warnings

RITE AID DAILY MOISTURIZER by is a Otc medication manufactured, distributed, or labeled by Rite Aid Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

• AVOBENZONE 3%
• OCTINOXATE 7.5%
• OCTISALATE 2%
  
  

Purpose

Sunscreen

WARNINGS

• FOR EXTERNAL USE ONLY.
  

WHEN USING THIS PRODUCT

AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE EYE THOROUGHLY WITH WATER TO REMOVE.

STOP USE AND ASK A DOCTOR IF

RASH OR REDNESS DEVELOPS AND LASTS.

KEEP OUT OF REACH OF CHILDREN

IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

OTHER INFORMATION

STORE AT ROOM TEMPERATURE.

USES

• HELPS PREVENT SUNBURN.
• HIGHER SPF GIVES MORE SUNBURN PROTECTION.
  

DIRECTIONS

APPLY EVENLY BEFORE SUN EXPOSURE. AFTER CLEANSING, SMOOTH OVER FACE AND NECK DAILY FOR HEALTHIER, YOUNGER LOOKING SKIN.

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 lotion

Product 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)