Label: FIRST AID ONLY ALCOHOL ANTISEPTIC PAD- alcohol 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 January 22, 2019

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  • Active Ingredients

    Active Ingredients Isopropyl Alcohol 70%

  • Purpose

    Antispetic Cleanser

  • Uses

    Uses •For preparation of the skin prior to injection

  • Warnings

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

  • Do Not Use

    Do not use • with electrocautery procedures

    •In the eyes. If contact occurs, flush eyes with water

  • Stop use

    Stop Use if irritation or redness develop.If condition persists consult your health care practicioner.

  • Keep out of reach of children

    Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center right away.

  • Directions

    Directions •Wipe Injection site vigorously and discard.

  • Inactive Ingredients

    Inactive Ingredients purified water

  • Package Label Principal Display Panel

    Carton LabelPackage Label

  • INGREDIENTS AND APPEARANCE
    FIRST AID ONLY ALCOHOL ANTISEPTIC PAD 
    alcohol pad swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0924-0009(NDC:71310-200)
    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:0924-0009-001 g in 1 PACKET; Type 0: Not a Combination Product07/26/2017
    2NDC:0924-0009-01100 in 1 CARTON06/28/2018
    21 g in 1 PACKET; Type 0: Not a Combination Product
    3NDC:0924-0009-02200 in 1 CARTON06/28/2018
    31 g in 1 PACKET; Type 0: Not a Combination Product
    4NDC:0924-0009-0310 in 1 CARTON01/22/2019
    41 g in 1 PACKET; Type 0: Not a Combination Product
    5NDC:0924-0009-0420 in 1 CARTON01/22/2019
    51 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 finalpart333A07/26/2017
    Labeler - Acme United Corporation (001180207)
    Establishment
    NameAddressID/FEIBusiness Operations
    Acme United Corporation045924339relabel(0924-0009) , repack(0924-0009)
    Establishment
    NameAddressID/FEIBusiness Operations
    Acme United Corporation080119599repack(0924-0009) , relabel(0924-0009)
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