RITE AID DAILY MOISTURIZER description, usages, side effects, indications, overdosage, supplying and lots more!

RITE AID DAILY MOISTURIZER

Rite Aid Corporation

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert
DRUG FACTS BOX

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENTS

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

Purpose

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

PACKAGE LABEL AND CARTON
PACKAGE LABEL AND CARTON
PACKAGE LABEL AND CARTON

RITE AID DAILY MOISTURIZER

AVOBENZONE LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:11822-6010
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
AVOBENZONE AVOBENZONE 3 mL
OCTINOXATE OCTINOXATE 7.5 mL
OCTISALATE OCTISALATE 2 mL

Inactive Ingredients

Ingredient Name Strength
ARACHIDYL ALCOHOL
docosanol
benzalkonium chloride
BENZYL ALCOHOL
BUTYLATED HYDROXYTOLUENE
BUTYLPARABEN
C12-15 ALKYL BENZOATE
C13-14 ISOPARAFFIN
DIMETHICONE
EDETATE DISODIUM
ETHYLPARABEN
GLYCERIN
SOYBEAN
isobutylparaben
LAURETH-7
METHYLPARABEN
MICA
PANTHENOL
PHENOXYETHANOL
PROPYLPARABEN
SILICON DIOXIDE
laureth-2
titanium dioxide
water
SODIUM HYDROXIDE
CITRIC ACID MONOHYDRATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:11822-6010-0 118 in 1 BOTTLE, PUMP
2 NDC:11822-6010-4 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2010-08-04


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