Label: WIPES PLUS- alcohol swab

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not 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 14, 2022

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  • Active Ingredient

    Alcohol 70% by volume

  • Purpose

    Antiseptic

  • Uses

    • For hand sanitizing to decrease bacteria on the skin.
    • Apply topically to the skin to help prevent cross contamination.
    • Recommended for repeated use.
    • Dries In seconds.

  • Warnings

    • Flammable, keep away from fire or flame. For external use only.
    • Do not use In or contact the eyes.
    • Discontinue use If redness or Irritation develops.
    • If condition persists for more than 72 hours, consult a physician.

    Keep our of reach of children

    Keep out of reach of chlldren unless under adult supervision.

  • Directions

    •Remove lld.
    • Pull wipe from center of roll and thread through opening in lid. Do not
    push finger through opening.
    • Replace lld, pull wipe up, and then out at 45 • angle. The next wipe
    dispenses automatically.
    • Close lld to retain moisture.

  • Inactive Ingredients

    Water, Propylene Glycol, Glycerin, Carboner, Aminomethyl Propanol, Aloe Barbadenis Leaf Juice, Tocopheryl Acetate.

  • Questions or Comments

    Lot No. and Expiration Date can be found on canister.

    @PROGRESSIVE PRODUCTS, LLC
    4 International Drive, Rye Brook, NY 1 0573
    CGll 914-417-6022
    Re-order/Item No. 33884
    www.wlpesplus.com

  • Principal Display Panel

    NDC 67151-606-01

    RE-ORDER/ITEM NO 37604

    Label

    NDC 67151-606-02

    RE-ORDER/ITEM NO 33884

    Label 1

    NDC 67151-606-03

    RE-ORDER/ITEM NO 37524

    Label 2

  • INGREDIENTS AND APPEARANCE
    WIPES PLUS 
    alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67151-606
    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)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67151-606-0180 in 1 PACKAGE09/01/2020
    11 mL in 1 PACKAGE; Type 0: Not a Combination Product
    2NDC:67151-606-02240 in 1 PACKAGE09/01/2020
    21 mL in 1 PACKAGE; Type 0: Not a Combination Product
    3NDC:67151-606-031500 in 1 PACKAGE09/01/2020
    31 mL in 1 PACKAGE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E09/01/2020
    Labeler - Progressive Products, LLC (127111792)
    Registrant - Progressive Products, LLC (127111792)
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