Label: ALCOHOL PREP PADS- 70%isopropyl alcohol swab

  • NDC Code(s): 82098-814-10
  • Packager: Raya Pharmaceuticals LLC
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated October 27, 2023

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  • INDICATIONS & USAGE

    For the preparation of the skin prior to an injection

    Wipe injection site vigorously and discard

    Alcohol Swab

  • PRECAUTIONS

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

  • WARNINGS AND PRECAUTIONS

    Warnings

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

    Stop Use

    · If irritation and redness develop.
    · If the 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.

  • STORAGE AND HANDLING

    Store at room temperature

    Protect from freezing. Avoid excessive heat.

  • Dosage and Administration

    Wipe injection site vigorously and discard

  • WARNINGS

    For External Use

    Flamable, Keep Away from fire and flame

  • Inactive ingredients

    Water

  • Keep out of reach of children

    Keep out of reach of children, if swallowed get medical help or contact a poison center right away.

  • Purpose section

    Use for preperation of the skin prioir to an injection

    Isopropyl Alcohol 70%........................Purpose: Antiseptic

  • Active ingredients

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

  • PRINCIPAL DISPLAY PANEL

    ALCOHOL PREP PAD

    Saturated with 70% Isopropyl Alcohol

    100 Swabs

    For External use only

    Principal Display Image

  • INGREDIENTS AND APPEARANCE
    ALCOHOL PREP PADS 
    70%isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82098-814
    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)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82098-814-100.7 mL in 1 POUCH; Type 0: Not a Combination Product03/12/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00303/12/2022
    Labeler - Raya Pharmaceuticals LLC (106631637)
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