Label: UP AND UP ACNE WASH- salicylic acid liquid

  • 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 August 6, 2021

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  • Active ingredient

    Salicylic Acid 2.0%

  • Purpose

    Acne Treatment

  • Uses

    for the treatment of acne.

  • Warnings

    For external use only

  • When using this product

    • skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs only use one topical acne medication at a time. • avoid contact with eyes. If contact occurs, flush thoroughly with water.

  • Keep out of reach of children.

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

  • Directions

    • cover the entire affected area with a thin layer and rinse thoroughly one to three times daily • if bothersome dryness or peeling occurs, reduce application to once a day or every other day • because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor.

  • Other information

    • may stain some fabric

  • Inactive ingredients

    Water, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Chamomilla Recutita (Matricaria) Flower Extract, Cocamidopropyl PG-Dimonium Chloride Phosphate, Propylene Glycol, Aloe Babadensis Leaf Juice, Anthemis Nobilis Flower Extract, C12-C15 Alkyl Lactate, PEG-80 Sorbitan Laurate, Disodium EDTA, Benzalkonium Chloride, Fragrance, Yellow 5, Red 40.

  • PRINCIPAL DISPLAY PANEL

    82713E1 82715F

    82713E 82714F

  • INGREDIENTS AND APPEARANCE
    UP AND UP  ACNE WASH
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-024
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
    PEG-80 SORBITAN LAURATE (UNII: 239B50Y732)  
    C12-15 ALKYL LACTATE (UNII: GC844VRD7E)  
    CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CHAMOMILE (UNII: FGL3685T2X)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-024-54269.1 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/24/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333D10/25/2013
    Labeler - TARGET CORPORATION (006961700)
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