Label: SINGULAR WIPES LAVENDER FRAGRANCE- alcohol cloth

  • NDC Code(s): 81428-072-01, 81428-072-02
  • Packager: SINGULAR ENTERPRISES LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 10, 2023

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  • Active Ingredient (s)

    Ethyl alcohol 70%

  • Purpose

    Antiseptic

  • Uses

    • Hand sanitizing to decrease bacteria on skin.
    • Recommended for repeated use.
  • Warnings

    • For external use only.
    • Flammable, keep away from fire or flame.
    • Do not use this product in or near eyes. If contact occurs, rinse thoroughly with water.
    • Keep out of reach of children unless under adult supervision.
    • Discontinue use if skin irritation and redness develop.
    • If condition persists for more than 72 hours consult a physician.
  • Directions

    • Tear open package and unfold wipe.
    • Thoroughly wipe hands fingers and wrists.
    • Be sure to use entire wipe for approximately 20 seconds.
    • No rinsing or toweling is required.
    • Discard after single use. Do not flush.
  • Inactive Ingredients.

    Purified Water (Aqua), glycerine, hydrogen peroxide,lavender fragrance.

  • Other information (if applicable)

    • Store below 104°F. (40°)
    • May discolor some fabrics.
  • KEEP OUT OF REACH OF CHILDREN

  • Product label

    image description

  • INGREDIENTS AND APPEARANCE
    SINGULAR WIPES LAVENDER FRAGRANCE 
    alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81428-072
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYDROGEN PEROXIDE (UNII: BBX060AN9V)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    LINALYL ACETATE (UNII: 5K47SSQ51G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81428-072-0130 in 1 BOX04/22/2022
    14 mL in 1 POUCH; Type 0: Not a Combination Product
    2NDC:81428-072-02100 in 1 BOX04/22/2022
    24 mL in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00304/21/2022
    Labeler - SINGULAR ENTERPRISES LLC (117830108)
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