Label: UP AND UP DEEP CLEAN TONER- 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 October 3, 2022

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  • Active ingredient

    Salicylic Acid 0.5%

  • 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

    • clean the skin thoroughly before using this product • cover the entire affected area with a thin layer one to three times daily • 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 doctor • if bothersome dryness or peeling occurs, reduce application to once a day or every other day.

  • Other information

    • may stain some fabric

  • Inactive ingredients

    water, alcohol denat. (24.5 %), glycerin, isoceteth-20, PEG-32, sodium citrate, fragrance, propylene glycol, dimethicone propyl PG-betaine, benozphenone-4, algae extract, aloe barbadenis leaf juice, blue 1

  • PRINCIPAL DISPLAY PANEL

    Up & Up Deep Clean Toner

    8 FL OZ (236.5 mL)

    NDC 11676-936-11

    82378E3

    82378F4

  • INGREDIENTS AND APPEARANCE
    UP AND UP  DEEP CLEAN TONER
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-936
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)  
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    POLYETHYLENE GLYCOL 1600 (UNII: 1212Z7S33A)  
    PHYMATOLITHON CALCAREUM (UNII: 6J1M3WA0ZK)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SULISOBENZONE (UNII: 1W6L629B4K)  
    ISOCETETH-20 (UNII: O020065R7Z)  
    DIMETHICONE PROPYL PG-BETAINE (UNII: OB83A4S9K9)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-936-11236.5 mL in 1 BOTTLE; Type 0: Not a Combination Product06/13/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333D06/13/2014
    Labeler - TARGET CORPORATION (006961700)
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