Label: ULTRA PREP ALCOHOL PREP PADS- isopropyl alcohol cloth

  • NDC Code(s): 83878-101-11
  • Packager: Quality Medical Products USA, Inc.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated July 16, 2024

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  • Drug Facts

  • Active ingredient

    Isopropyl Alcohol, 70% v/v

  • Purpose

    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 or redness develop. If your condition persists for more than 72 hours, consult a doctor.

    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 after single use.

  • Inactive ingredient

    purified water

  • SPL UNCLASSIFIED SECTION

    Saturated with 70% isopropyl Alcohol. 

    USE: For skin cleaning prior to injection.

    DIRECTION: Rub skin briskly in a circular motion from injection site outward.

    CAUTION EXTERNAL USE ONLY: In the event of skin irritation or rash, discontinue use. Avoid contact with eyes, if contacted, flush eyes with copious amount of water. If ingested, DO NOT induce vomiting, obtain medical attention immediately.

    Quality Medical Products, USA
    545 NW Mercantile Place
    Unit 115 Port St Lucie, Fl 34986
    info@qualitymedusa.com
    800.488.1370

    Made in China

  • Packaging

    UltraPrepPad-101

  • INGREDIENTS AND APPEARANCE
    ULTRA PREP ALCOHOL PREP PADS 
    isopropyl alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83878-101
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83878-101-11100 in 1 BOX07/15/2024
    11 in 1 PACKET
    10.45 mL in 1 PACKAGE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)07/15/2024
    Labeler - Quality Medical Products USA, Inc. (054180248)
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