Label: ALCOHOL PREP- isopropyl alcohol swab

  • NDC Code(s): 67777-121-11, 67777-121-12, 67777-121-13, 67777-121-14, view more
    67777-121-16, 67777-121-17, 67777-121-18, 67777-121-19, 67777-121-20, 67777-121-21, 67777-121-22, 67777-121-23, 67777-121-24, 67777-121-26, 67777-121-27
  • Packager: Dynarex Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 12, 2024

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  • Active Ingredient

    Isopropyl Alcohol 70%


  • Purpose

    Antiseptic

  • Use(s)

    • First aid to help prevent infection in minor cuts, scrapes, and burns

    • For preparation of the skin prior to an injection

  • Warnings

    For External Use only

    Flammable. Keep away from fire or flame.

    Do not use

    • In the eyes or over large areas of the body

    • Longer than 1 week unless directed by a doctor

    • With electrocautery procedures


    Ask a doctor before use if you have

    Deep or puncture wounds, animal bites, or serious burns.

    Stop use and ask a doctor if

    Condition persists for more than 72 hours or gets worse.

    Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • Directions

    • When used for first aid: Clean the affected area. Apply a small amount of this product on the area 1 to 3 times daily. May be covered with a sterile bandage. If bandaged, let dry first.

    • When used to prepare an injection site: Apply product to the injection site prior to injection.

  • Other Information

    • Store at room temperature
    • Avoid excessive heat
  • Inactive Ingredient

    Water


  • Label

    1113-1116 Box Master

  • Label 1113-50

    1113-50_BX_MASTER1113-50

  • Label 1113UB-24

    1113UB-2 BX_MASTER1113UB-24

  • Label 1113UB-10

    1113UB-10_BX_MASTER1113UB-10

  • INGREDIENTS AND APPEARANCE
    ALCOHOL PREP 
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-121
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    Color    Score    
    ShapeRECTANGLESize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67777-121-2020000 in 1 CASE07/01/2010
    1NDC:67777-121-19100 in 1 BOX
    1NDC:67777-121-140.55 mL in 1 POUCH; Type 0: Not a Combination Product
    2NDC:67777-121-181000 in 1 CASE07/01/2010
    2NDC:67777-121-17100 in 1 BOX
    2NDC:67777-121-160.7 mL in 1 POUCH; Type 0: Not a Combination Product
    3NDC:67777-121-122000 in 1 CASE07/01/2010
    3NDC:67777-121-11200 in 1 BOX
    3NDC:67777-121-130.55 mL in 1 POUCH; Type 0: Not a Combination Product
    4NDC:67777-121-261000 in 1 CASE07/01/2010
    4NDC:67777-121-2750 in 1 BOX
    40.55 mL in 1 POUCH; Type 0: Not a Combination Product
    5NDC:67777-121-22480 in 1 CASE07/01/2010
    5NDC:67777-121-2124 in 1 BOX
    50.55 mL in 1 POUCH; Type 0: Not a Combination Product
    6NDC:67777-121-241000 in 1 CASE07/01/2010
    6NDC:67777-121-2310 in 1 BOX
    60.55 mL in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00307/01/2010
    Labeler - Dynarex Corporation (008124539)
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