Label: ALCOHOL PAD- alcohol prep pad 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 December 11, 2019

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  • Active Ingredient (in each towelette) ............Purpose

    Isopropyl Alcohol 70%..........Antiseptic

  • Use:

    For preparation of skin prior to 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 consult your health care practitioner.

    Keep out of reach of children.

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

  • Directions:

    Wipe injection area and discard.

  • Other information:

    Store at room temperature 15 o to 30 oC (59 o to 86 oF).

  • Inactive ingredient:

    water

  • PRINCIPAL DISPLAY PANEL

    BoxPacket

  • INGREDIENTS AND APPEARANCE
    ALCOHOL PAD 
    alcohol prep pad swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71105-111
    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)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71105-111-0350 in 1 BOX03/31/2017
    1NDC:71105-111-021 in 1 PACKET
    1NDC:71105-111-010.45 g in 1 PATCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/31/2017
    Labeler - Redicare LLC (800149346)
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