Label: ALCOHOL PREP- isopropyl alcohol cloth

  • NDC Code(s): 71310-005-01
  • Packager: Taizhou Kangping Medical Science And Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 14, 2023

If you are a consumer or patient please visit this version.

  • Drug Facts

  • Active Ingredients

    Isopropyl Alcohol 70% V/V

    Purpose

    Antiseptic

  • Use

    • For preparation of the skin prior to injection and to decrease germs in minor cuts and scrapes.
    • Non-sterile Solution.
    • Applicator is sterile if package is intact
  • Warnings

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

    Do not use

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

    Stop use

    If irritation and redness develops and persists for more than 72 hours, consult your health care practitioner.

    Keep out of reach of children

    Except with adult supervision. If swallowed, get medical help or contact a poison control center right away

  • Directions

    • Apply topically as needed to cleanse intended area.
    • Discard after single use.
  • Other information

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

  • Inactive ingredients

    Purified water.

  • Package Labeling:

    alcohol prep pad

  • INGREDIENTS AND APPEARANCE
    ALCOHOL PREP 
    isopropyl alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71310-005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL700 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71310-005-01100 in 1 BOX11/11/2018
    11 in 1 PACKAGE
    10.4 mL in 1 PACKAGE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00311/11/2018
    Labeler - Taizhou Kangping Medical Science And Technology Co., Ltd. (543429840)
    Establishment
    NameAddressID/FEIBusiness Operations
    Taizhou Kangping Medical Science And Technology Co., Ltd.543429840manufacture(71310-005)