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 February 4, 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



    Ask a doctor

    if 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

    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

    Sunmark®

    COMPARE TO B-D® ACTIVE INGREDIENTS*

    NDC 49348-077-53

    Alcohol Prep Pads

    Antiseptic for preparation of the skin prior to injection

    Isopropyl alcohol, 70%

    100 INDIVIDUALLY WRAPPED FOIL PACKETS
    1.25 X 1.25 IN (2.9 X 3.2 cm)

    Distributed by McKesson
    One Post Street
    San Francisco, CA 94104
    Money Back Guarantee

    *This product is not namufactured or distributed by Beckton Dickson, owner of the registered trademark, B-D®.


    image of carton
  • INGREDIENTS AND APPEARANCE
    ALCOHOL PAD 
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49348-077
    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:49348-077-53100 in 1 BOX
    11 in 1 PACKET
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E06/19/2003
    Labeler - McKesson (177667227)
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