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

Up and Up by

Drug Labeling and Warnings

Up and Up by is a Otc medication manufactured, distributed, or labeled by TARGET CORPORATION. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

Do not use on damaged or broken skin.

WHEN USING

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

STOP USE

Stop use and ask a doctor if rash occurs.

KEEP OUT OF REACH OF CHILDREN

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

PRINCIPAL DISPLAY PANEL

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

INGREDIENTS AND APPEARANCE

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

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	20 mg  in 1 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	75 mg  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
GLYCOL DILAURATE (UNII: 9O691KKR2A)
PEG-4 LAURATE (UNII: AYF4VM3N1Z)
BENZYL ALCOHOL (UNII: LKG8494WBH)
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S) (UNII: 1PEZ3NLY6I)
POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)
ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
DIMETHICONE (UNII: 92RU3N3Y1O)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
SOYBEAN OIL (UNII: 241ATL177A)
PANTHENOL (UNII: WV9CM0O67Z)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
STEARETH-21 (UNII: 53J3F32P58)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
POLYETHYLENE GLYCOL 200 (UNII: R95B8J264J)
GLYCERIN (UNII: PDC6A3C0OX)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
WATER (UNII: 059QF0KO0R)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
DOCOSANOL (UNII: 9G1OE216XY)
MICA (UNII: V8A1AW0880)
LAURETH-7 (UNII: Z95S6G8201)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
STEARETH-2 (UNII: V56DFE46J5)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11673-934-05	1 in 1 CARTON	10/04/2019
1	NDC: 11673-934-04	118.3 mL in 1 BOTTLE; Type 0: Not a Combination Product

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	Business Operations
Fruit Of The Earth Research Laboratories, Inc.		008193513	manufacture(11673-934)