Label: SAFE CLEAN WET WIPE- ethyl alcohol 75% 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 June 30, 2020

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  • Active Ingredient

    Ethyl Alcohol 75%

  • Purpose

    Antibacterial

  • Uses

    To help reduce bacteria on the skin.

  • Warnings

    For External Use only. Do not dispose of wipes in flush toilets. Flammable. Keep away from heat or flame.

  • When using this product

    Avoid contact with eyes. If contact occurs, rinse thoroughly with water.

  • ­­­­­­­­­­­­­­­­­­­Stop use and ask a doctor.

    If irritation or redness develops and last.

  • Keep out of reach of children.

    In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

  • ­­­­­­­­­­­­­­­­­­­­­Directions

    Apply to hands or skin. No rinsing require/ Discard after use.

  • Other Information

    Store below 110F (43C)

    May discolor certain fabrics or surfaces.

  • Inactive Ingredients

    Aqua (Water), Glycerin, Polyquaternium-37, Melaleuca Alternifolia Leaf Oil.

  • Safe + Clean Wet wipe

    label

  • INGREDIENTS AND APPEARANCE
    SAFE CLEAN WET WIPE 
    ethyl alcohol 75% swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79312-102
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.75 mL
    Inactive Ingredients
    Ingredient NameStrength
    MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYQUATERNIUM 37 (200 MPA.S) (UNII: 67C1D6YV24)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79312-102-011 in 1 BAG; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug05/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A05/01/2020
    Labeler - Mimish Designs, LLC (131433402)
    Registrant - Mimish Designs, LLC (131433402)
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