TARGET UP AND UP SPF 50 MINERAL SUNSCREEN- titanium dioxide, zinc oxide 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.

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Target Up & Up SPF 50 Mineral Sunscreen Lotion

Active ingredients

Titanium Dioxide 3.0%

Zinc Oxide 15.0%

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 skin 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

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

• limit time in the sun, especially from 10 a.m. - 2 p.m.

• wear long-sleeved shirts, pants, hats, and sunglasses

Other information

• protect the product in this container from excessive heat and direct sun

• may stain or damage some fabrics, materials or surfaces

Inactive ingredients

Water, Caprylic/Capric Triglyceride, Neopentyl Glycol Diheptanoate, Butyloctyl Salicylate, Glycerin, Olive Oil Polyglyceryl-6 Esters, C30-38 Olefin/Isopropyl Maleate/MA Copolymer, Phenoxyethanol, Polyglyceryl-6 Pentaoleate, Stearyl/Octyldodecyl Citrate Crosspolymer, VP/Hexadecene Copolymer, Glyceryl Stearate, Magnesium Sulfate, Silica, Simmondsia Chinensis (Jojoba) Seed Oil, Ethylhexylglycerin, Aloe Barbadensis Leaf Juice, Avena Sativa (Oat) Kernel Extract, Tocopherol, Sodium Hydroxide.

Label

82076E1F1

82061EF

82060A1

82073F

TARGET UP AND UP SPF 50 MINERAL SUNSCREEN 
titanium dioxide, zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-233
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE150 mg  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE30 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
MAGNESIUM SULFATE HEPTAHYDRATE (UNII: SK47B8698T)  
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)  
OLIVE OIL POLYGLYCERYL-6 ESTERS (UNII: 4KDO9AFM9I)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
GLYCERYL 1-STEARATE (UNII: 258491E1RZ)  
JOJOBA OIL (UNII: 724GKU717M)  
STEARYL/OCTYLDODECYL CITRATE CROSSPOLYMER (UNII: PN88NW0KPK)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
.ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01)  
VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)  
WATER (UNII: 059QF0KO0R)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
GLYCERIN (UNII: PDC6A3C0OX)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
OATMEAL (UNII: 8PI54V663Y)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-233-15177 mL in 1 TUBE; Type 0: Not a Combination Product09/22/2020
2NDC:11673-233-40307.5 mL in 1 BOTTLE; Type 0: Not a Combination Product09/22/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalM02009/22/2020
Labeler - TARGET CORPORATION (006961700)

Revised: 4/2023
Document Id: f9902a2a-6fbb-49e9-e053-6294a90a338c
Set id: f99028fa-a17e-4a84-e053-6294a90a927f
Version: 1
Effective Time: 20230417
 
TARGET CORPORATION