TARGET UP AND UP MORNING FACIAL MOISTURIZING WITH SUNSCREEN BROAD SPECTRUM SPF 30- homosalate, octocrylene, 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 and Up Morning Facial Moisturizing Lotion with Sunscreen Broad Spectrum SPF 30

Active ingredients

Homosalate15.0%, Octocrylene 2.0%, Zinc Oxide 6.3%

Purpose

Sunscreen

Uses

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

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

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

Other information

Inactive ingredients

Water, Niacinamide, Glycerin, Cetearyl Alcohol, Dimethicone, Cetearyl Glucoside, Ceramide NP, Ceramide AP, Ceramide EOP, Sodium Hyaluronate, Aluminum Starch Octenylsuccinate, Boron Nitride, Hydroxyethylcellulose, Disodium EDTA, Cetyl Palmitate, Sorbitan Palmitate, Sorbitan Olivate, Phenoxyethanol, Capryloyl Glycine, Undecylenoyl Glycine, Triethoxycaprylylsilane, Sodium Lauroyl Lactylate, Phytosphingosine, Cholesterol, Carbomer, Xanthan Gum.

Label

82910E1F3

82910K4

TARGET UP AND UP MORNING FACIAL MOISTURIZING WITH SUNSCREEN BROAD SPECTRUM SPF 30 
homosalate, octocrylene, zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-239
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE150 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE63 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
CERAMIDE NP (UNII: 4370DF050B)  
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)  
SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)  
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
CERAMIDE AP (UNII: F1X8L2B00J)  
CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)  
CETYL PALMITATE (UNII: 5ZA2S6B08X)  
BORON NITRIDE (UNII: 2U4T60A6YD)  
CHOLESTEROL (UNII: 97C5T2UQ7J)  
HEXAMETHYLDISILOXANE (UNII: D7M4659BPU)  
HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16)  
PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
SORBITAN MONOPALMITATE (UNII: 77K6Z421KU)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
UNDECYLENOYL GLYCINE (UNII: 4D20464K2J)  
NIACINAMIDE (UNII: 25X51I8RD4)  
SORBITAN OLIVATE (UNII: MDL271E3GR)  
XANTHAN GUM (UNII: TTV12P4NEE)  
POLYACRYLIC ACID (8000 MW) (UNII: 73861X4K5F)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-239-031 in 1 CARTON10/13/2015
189 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalM02010/13/2015
Labeler - TARGET CORPORATION (006961700)

Revised: 4/2023
Document Id: f9b6a393-6ffa-d0b1-e053-6394a90ab5c8
Set id: f9b66e3e-5493-9ea4-e053-6294a90a6063
Version: 1
Effective Time: 20230419
 
TARGET CORPORATION