Up and Up Illuminating Daily Moisturizer with Sunscreen Broad Spectrum SPF 15: Package Insert and Label Information

UP AND UP ILLUMINATING DAILY MOISTURIZER WITH SUNSCREEN BROAD SPECTRUM SPF 15- octisalate, octinoxate and avobenzone lotion
TARGET CORPORATION

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.

Up and Up Illuminating Daily Moisturizer with Sunscreen Broad Spectrum SPF 15

Active ingredients

Avobenzone 3.0%, Octinoxate 7.5%, Octisalate 2.0%

Purpose

Sunscreen

Uses

  • helps prevent sunburn
  • if used as directed with other sun protection measures (see Directions ), decreases the risk of skin cancer and early aging caused by the sun

Warnings

For external use only

Do not use • on damaged or broken skin.

When using this product ​• keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if • rash occurs.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • apply liberally 15 minutes before sun exposure.
  • reapply:
  • after 80 minutes of swimming or sweating
  • immediately after towel drying
  • at least every 2 hours
  • children under 6 months of age: ask a doctor
  • Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad-spectrum SPF of 15 or higher and other sun protection measures including:
  • limit time in the sun especially from 10 a.m. – 2 p.m.
  • wear long-sleeve shirts, pants, hats, and sunglasses

Other information

  • protect this product from excessive heat and direct sun
  • may stain or damage some fabrics, materials or surfaces

Inactive ingredients

Water, C12-15 Alkyl Benzoate, Glycerin, Cetearyl Alcohol, Dimethicone, Glycine Soja (Soybean) Seed Extract, Phenyl Trimethcione, Arachidyl Alcohol, Cetearyl Glucoside, Phenoxyethanol, Benzyl Alcohol, Panthenol, Ethylene/ Acrylic Acid Copolymer, Behenyl Alcohol, Steareth-2, Fragrance, Steareth-21, Polymethyl Methacrylate, Polyacrylamide, Arachidyl Glucoside, Disodium EDTA, C13-14 Isoparaffin, Laureth-7, Silica, Benzalkonium Chloride, Iodopropynyl Butylcarbamate, PEG-4 Dilaurate, PEG-4 Laurate, PEG-4, Alcohol, BHT, Sodium Hydroxide, Citric Acid, Titanium Dioxide, Mica

Questions or comments?

Call toll free 1-800-910-6874

Up and Up Illuminating Daily Moisturizer with Sunscreen Broad Spectrum SPF 15

4 FL OZ (118.3 mL)

NDC 11673-934-04 Bottle

NDC 11673-934-05 Carton

Label
(click image for full-size original)
UP AND UP ILLUMINATING DAILY MOISTURIZER WITH SUNSCREEN BROAD SPECTRUM SPF 15
avobenzone, octinoxate, octisalate lotion
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-934
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
OCTISALATE (OCTISALATE) OCTISALATE 20 mg in 1 mL
OCTINOXATE (OCTINOXATE) OCTINOXATE 75 mg in 1 mL
AVOBENZONE (AVOBENZONE) AVOBENZONE 30 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
TITANIUM DIOXIDE
GLYCOL DILAURATE
PEG-4 LAURATE
BENZYL ALCOHOL
C13-14 ISOPARAFFIN
ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S)
POLYACRYLAMIDE (1500 MW)
ARACHIDYL GLUCOSIDE
DIMETHICONE
BENZALKONIUM CHLORIDE
SOYBEAN OIL
PANTHENOL
SODIUM HYDROXIDE
STEARETH-21
CETOSTEARYL ALCOHOL
ARACHIDYL ALCOHOL
PHENYL TRIMETHICONE
SILICON DIOXIDE
POLY(METHYL METHACRYLATE; 450000 MW)
POLYETHYLENE GLYCOL 200
GLYCERIN
EDETATE DISODIUM (EDETIC ACID)
ANHYDROUS CITRIC ACID
ALKYL (C12-15) BENZOATE
WATER
BUTYLATED HYDROXYTOLUENE
CETEARYL GLUCOSIDE
DOCOSANOL
MICA
LAURETH-7
PHENOXYETHANOL
IODOPROPYNYL BUTYLCARBAMATE
STEARETH-2
ALCOHOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:11673-934-05 1 BOTTLE in 1 CARTON contains a BOTTLE (11673-934-04)
1 NDC:11673-934-04 118.3 mL in 1 BOTTLE This package is contained within the CARTON (11673-934-05)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part352 10/04/2019
Labeler — TARGET CORPORATION (006961700)
Registrant — Fruit Of The Earth, Inc. (079559467)
Establishment
Name Address ID/FEI Operations
Fruit Of The Earth Research Laboratories, Inc. 008193513 manufacture (11673-934)

Revised: 10/2019 TARGET CORPORATION

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