Label: TARGET UP AND UP DAILY MOISTURIZING- dimethicone lotion

  • NDC Code(s): 11673-087-18, 11673-087-43, 11673-087-98
  • 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 10, 2023

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  • Active ingredients

    Dimethicone 1.2%

  • Purpose

    Skin Protectant

  • 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

    • deep or puncture wounds • animal bites • serious burns

  • When using this product

    • keep out of eyes. Rinse with water to remove.

  • Stop use and ask a doctor if

    • condition worsens • symptoms last more than seven days or clear up and occur again within a few days

  • Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • apply as needed to hands or body when skin feels dry or irritated
  • Other information

    • may stain some fabrics
  • Inactive ingredients

    avena sativa (oat) kernel flour, behenrimonium chloride, benzyl alcohol, cetearyl alcohol, cetyl alcohol, glycerin, isopropyl palmitate, petrolatum, polyquaterium-37, sodium chloride, water.

  • Label

    82845E8F9

  • INGREDIENTS AND APPEARANCE
    TARGET UP AND UP DAILY MOISTURIZING 
    dimethicone lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-087
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE12 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    POLYQUATERNIUM 37 (200 MPA.S) (UNII: 67C1D6YV24)  
    BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    OATMEAL (UNII: 8PI54V663Y)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-087-1885 mL in 1 TUBE; Type 0: Not a Combination Product05/01/2009
    2NDC:11673-087-982 in 1 PACKAGE05/01/2009
    2NDC:11673-087-43532 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalM01605/01/2009
    Labeler - TARGET CORPORATION (006961700)
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