Label: ACP ANTIBACTERIAL ALCOHOL WIPES- ethyl alcohol cloth

  • 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 July 9, 2020

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

  • Drug Facts

  • Active Ingredient

    Ethyl Alcohol 70%

  • Purpose

    Antiseptic Handwash

  • Uses

    · For hand washing to decrease bacteria on the skin.

      Store in a cool, dry place

  • Directions

    · Wet hands thoroughly with product and allow to dry without wiping.

  • Other Information

    · Do not store above 110°F

    · May discolor some fabrics

  • Warnings

    For external use only,

    Do not use- in mouth or touch eyes

    Non-flushable

    Flammable - Keep away from fire or flame

    When using this product, avoid contact with eyes. In case of eye contact, rinse with water to remove.

    Stop use and ask a doctor if irritation and redness develop. 

    Keep out of reach of children

  • Inactive Ingredients

    Aqua,Glycerin,Aloe Barbadensis Leaf Juice.

  • SPL UNCLASSIFIED SECTION

    With 70% Alcohol

    √ Essential for home or outside

    √ Contains alcohol

    √ Used for hands and surface

    Marketed & distributed by Swanrose Inc.

    Address:SWANROSE, INC.

    751 N. SPAULDING AVENUE

    LOS ANGELES, CA 90046

    PHONE: +1 (310) 266-5812

    Shelf Life: 24 months

  • Packaging

    IMAGE

  • INGREDIENTS AND APPEARANCE
    ACP ANTIBACTERIAL ALCOHOL WIPES 
    ethyl alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78287-140
    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)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78287-140-021 in 1 POUCH06/25/2020
    13.57 mL in 1 PACKAGE; Type 0: Not a Combination Product
    2NDC:78287-140-0310 in 1 POUCH06/25/2020
    23.57 mL in 1 PACKAGE; Type 0: Not a Combination Product
    3NDC:78287-140-0150 in 1 POUCH06/25/2020
    33.57 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 finalpart333A06/25/2020
    Labeler - Swanrose, Inc. (117523391)