Label: ALCOHOL 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 March 15, 2010

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  • ACTIVE INGREDIENT

    Isopropyl Alcohol 70% v/v

  • PURPOSE

    Antiseptic

  • USE

    For preparation of the skin prior to an injection
  • WARNINGS

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

    Do not use

    • with electrocautery procedures
    • in the eyes

    Stop use

    if irritation and redness develop. If condition persists for more than 72 hours, consult a doctor.






    Keep out of reach of children

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

  • DIRECTIONS

    Wipe injection site vigorously and discard
  • SPL UNCLASSIFIED SECTION


  • OTHER INFORMATION

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

    purified water
  • QUESTIONS


  • PACKAGE INFORMATION

    The Medicine Shoppe®

    NDC 49614-622-78

    CONVENIENT TO USE

    ALCOHOL SWABS
    70% Isopropyl Alcohol

    Antiseptic for preparation
    of the skin prior to injection

    100% Satisfaction Guaranteed

    COMPARE TO B-D® ALCOHOL SWABS active ingredient*

    100 INDIVIDUALLY WRAPPED FOIL PACKETS

    Distributed by
    Medicine Shoppe International, Inc.
    Earth City, MO 63045
    www.medicineshoppe.com
    A Cardinal Health Company
    CIN 1126507
    1-800-325-1397


    image of carton
  • INGREDIENTS AND APPEARANCE
    ALCOHOL PAD 
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49614-622
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Isopropyl alcohol (UNII: ND2M416302) (Isopropyl alcohol - UNII:ND2M416302) Isopropyl alcohol0.70 mL
    Inactive Ingredients
    Ingredient NameStrength
    water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49614-622-78100 in 1 BOX
    11 in 1 PACKET
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E01/01/2004
    Labeler - Medicine Shoppe International Inc (071997654)
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