Label: UP AND UP OIL-FREE CLEANSING WIPE PINK GRAPEFRUIT- salicylic acid cloth

  • NDC Code(s): 11673-409-25, 11673-409-50
  • 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 June 25, 2020

If you are a consumer or patient please visit this version.

  • Active ingredient

    Salicylic acid 2%

  • Purpose

    Acne treatment

  • Uses

    • Treats acne.
    • Dries up acne pimples.

  • Warnings

    For external use only.

  • Keep out of reach of children.

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

  • When using this product

    • Skin irritaion and dryness are 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 the eyes. If product gets into eyes, rinse thoroughly with water.
  • Directions

    Open resealable label to access wipe; reseal label tightly to retain moisture. Thoroughly wipe face with cleansing cloth to deep clean and refresh skin. After use, dispose of wipe in trash receptable. Do not flush. Clean the skin thoroughly before applying this product.

  • Other information

    Lot Number and Expiration Date can be found on pack.

  • Inactive ingredients

    Alcohol Denat. Butylene Glycol, Citrus Grandis (Grapefruit) Fruit Extract, Disodium EDTA, Fragrance, Glycerin, Iodopropynyl Butylcarbamate, PEG-32, Phenoxyethanol, PPG-5-Ceteth-20, Sodium Citrate, Sodium Hydroxide, Sodium Xylenesulfonate, Water

  • Principal display panel

    reseal label

    reseal

    web

    web

    tray

    tray

  • INGREDIENTS AND APPEARANCE
    UP AND UP OIL-FREE CLEANSING WIPE   PINK GRAPEFRUIT
    salicylic acid cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-409
    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
    ALCOHOL (UNII: 3K9958V90M)  
    SODIUM XYLENESULFONATE (UNII: G4LZF950UR)  
    PPG-5-CETETH-20 (UNII: 4AAN25P8P4)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    WATER (UNII: 059QF0KO0R)  
    PEG-32 STEARATE (UNII: 33GX5WQC0M)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    GRAPEFRUIT (UNII: O82C39RR8C)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    DISODIUM EDTA-COPPER (UNII: 6V475AX06U)  
    GRAPEFRUIT JUICE (UNII: JQ9EK2H6BG)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-409-502 in 1 TRAY01/01/2017
    1NDC:11673-409-2525 in 1 CELLO PACK
    16.6 mL in 1 APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333D01/01/2017
    Labeler - Target Corporation (006961700)
    Registrant - Nice-Pak Products, Inc. (003778198)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nice-Pak Products, Inc.067900167manufacture(11673-409)