Label: SPECTRUM HAND SANITIZER WIPES- ethyl alcohol cloth

  • NDC Code(s): 53329-840-29, 53329-840-32, 53329-840-63
  • Packager: Medline Industries, LP
  • Category: HUMAN OTC DRUG LABEL

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 18, 2022

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  • Active ingredient

    Ethyl alcohol 70%

  • Purpose

    Antiseptic

  • Uses

    • to decrease bacteria on the skin that could cause disease
  • Warnings

    For external use only: hands

    Flammable. Keep away from fire and flame.

    When using this product

    • keep out of eyes. In case of contact with eyes, flush thoroughly with water.
    • avoid contact with broken skin
    • do not inhale or ingest

    Stop Use and ask a doctor if

    • irritation or redness develops
    • condition persists for more than 72 hours

    Keep out of reach of children.

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

  • Directions

    • wet hands thoroughly with product and allow to dry without wiping
    • not recommended for infants
  • Other information

    • do not store above 105ºF
    • may discolor some fabrics
    • harmful to wood finishes and plastics
  • Inactive ingredients

    aloe barbadensis leaf juice, glycerin, isopropanol, propanediol, tocopheryl acetate, water

  • Manufacturing Information

    Manufactured for:

    Medline Industries, LP

    Three Lakes Drive, Northfield, IL 60093 USA

    Made in USA

    www.medline.com

    1-800-MEDLINE (633-5463)

    REF: HH70W160

    V3 RG22GON

  • Packaging Label

    Label V3 RG22GON

  • INGREDIENTS AND APPEARANCE
    SPECTRUM HAND SANITIZER WIPES 
    ethyl alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53329-840
    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
    .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53329-840-3220 in 1 PACKAGE01/01/2019
    13.1 mL in 1 APPLICATOR; Type 0: Not a Combination Product
    2NDC:53329-840-2950 in 1 CANISTER01/01/201909/30/2022
    25.77 mL in 1 APPLICATOR; Type 0: Not a Combination Product
    3NDC:53329-840-63160 in 1 CANISTER01/01/2019
    32.77 mL in 1 APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/01/2019
    Labeler - Medline Industries, LP (025460908)
    Registrant - Medline Industries, LP (025460908)
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