Label: TARGET UP AND UP SPF55 SUNSCREEN REEF-CONSCIOUS FORMULA- avobenzone, homosalate, octisalate, octocrylene stick

  • NDC Code(s): 11673-135-01, 11673-135-28, 11673-135-36, 11673-135-56, view more
    11673-135-57, 11673-135-91
  • Packager: TARGET CORPORATION
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

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.

Drug Label Information

Updated April 7, 2023

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  • Active ingredients

    Avobenzone 3.0%

    Homosalate 15.0%

    Octisalate 5.0%

    Octocrylene 10.0%

  • 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

    • rash occurs.

  • Keep out of reach of children

    If product is swallowed, get medical help or contact a Poison Control 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 value 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-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

    beeswax (apis mellifera), lauryl laurate, ozokerite, cetearyl behenate, polybutene, butyloctyl salicylate, cetyl alcohol, styrene/acrylates copolymer, myristyl myristate, theobroma cacao (cocoa) seed butter, phenoxyethanol, tocopherol, tetrahexyldecyl ascorbate

  • Labels

    82456E1

    82026K

    82918EF

    82409E1

    82025E1F1

    82409K2

    82919K

    82918K

    82026EF

    82024E1F

  • INGREDIENTS AND APPEARANCE
    TARGET UP AND UP SPF55 SUNSCREEN REEF-CONSCIOUS FORMULA 
    avobenzone, homosalate, octisalate, octocrylene stick
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-135
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 g
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE150 mg  in 1 g
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE100 mg  in 1 g
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    POLYBUTENE (1400 MW) (UNII: 1NA5AO9GH7)  
    .ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    COCOA BUTTER (UNII: 512OYT1CRR)  
    LAURYL LAURATE (UNII: GPW77G0937)  
    CERESIN (UNII: Q1LS2UJO3A)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    WHITE WAX (UNII: 7G1J5DA97F)  
    STEARYL BEHENATE (UNII: A68S9UI39D)  
    MYRISTYL MYRISTATE (UNII: 4042ZC00DY)  
    ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-135-5734 in 1 PACKAGE01/15/2019
    1NDC:11673-135-5617 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:11673-135-9126.6 in 1 PACKAGE04/24/2019
    2NDC:11673-135-0113.3 g in 1 TUBE; Type 0: Not a Combination Product
    3NDC:11673-135-3684 in 1 PACKAGE04/24/2019
    3NDC:11673-135-2842 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalM02001/15/2019
    Labeler - TARGET CORPORATION (006961700)
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