Label: OPTIMAL ALCOHOL PREP PAD- isopropyl 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 June 28, 2018

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  • Active Ingredient

    Isopropyl Alcohol 70%

  • Purpose

    Antiseptic Cleanser

  • INDICATIONS & USAGE

    Apply topically as needed to cleanse

  • Warnings

    For external use only. Flammable, keep away from fire or flame.

  • Do Not Use

    With electrocautery procedures. In the eyes. If contact occurs, flush eyes with water.

  • Stop Use

    If irritation and redness develop. If condtion persists consult your health care practitioner.

  • Keep Out of Reach of Children

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

  • Other Information

    Store at room temperature 15°-30° C (59°-86° F)

  • Inactive Ingredient

    Purified water

  • DOSAGE & ADMINISTRATION

    For External Use Only

  • PRINCIPAL DISPLAY PANEL

    Top of Box

  • INGREDIENTS AND APPEARANCE
    OPTIMAL ALCOHOL PREP PAD 
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72347-070
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL70 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    Colorwhite (Packet wrapper is white with blue lettering) Score    
    ShapeRECTANGLESize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72347-070-02200 in 1 BOX02/25/2013
    1NDC:72347-070-011 g in 1 PACKET; Type 0: Not a Combination Product
    2NDC:72347-070-0320 in 1 CASE02/25/2013
    2NDC:72347-070-02200 in 1 BOX
    2NDC:72347-070-011 g in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A02/25/2013
    Labeler - Hilco Vision (001196872)
    Establishment
    NameAddressID/FEIBusiness Operations
    Hilco Vision001196872label(72347-070)
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