Label: 62% ETHYL ALCOHOL NASAL SWAB- ethyl alcohol nasal swab swab

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 5, 2024

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  • Active ingredient

    Ethyl alcohol 62% v/v

  • Purpose

    Antiseptic

  • Uses

    helps reduce bacteria that can cause skin infections

  • Warnings

    For external use only.

    flammable, keep away from open flame.

    Do not use

    -in the eyes

    -on children under 2 years of age unless directed by a doctor

    Ask doctor before use if injuries are

    -deep or puncture wounds

    -serious burns

    Stop use and ask doctor if

    -redness, irritation, swelling or pain persists or increase

    -infection occurs

    Keep out of reach of children

    In case of accidental ingestion, seek professional assistance or consult a poison control center immediately.

  • Directions

    Nasal Application:

    1. Use a tissue to clean inside both nostrils, including inside tip of nostil. Discard.

    2. Insert right swab comfortable into right nostil and rotate for 30 seconds, covering all surfaces. Discard swab.

    3. Using left swab repeat Step 2 with left nostril.

    4. Do not blow nose. If solution drips, gently wipe with a tissue.

  • Other Information

    -Store at room temperature

    -not made with natural rubber latex

    -for hospital or professional use only

  • Inactive ingredients

    ascorbyl palmitate, benzyl alcohol, BHT, castor (ricinus communis) oil, isopropyl alcohol, fragrance, menthol, polyaminopropyl biguanide, purified water

  • Label

    Entire Label

  • INGREDIENTS AND APPEARANCE
    62% ETHYL ALCOHOL NASAL SWAB 
    ethyl alcohol nasal swab swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83062-032(NDC:53329-032)
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEHYDRATED ALCOHOL (UNII: 3K9958V90M) (DEHYDRATED ALCOHOL - UNII:3K9958V90M) DEHYDRATED ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    CASTOR OIL (UNII: D5340Y2I9G)  
    WATER (UNII: 059QF0KO0R)  
    POLYAMINOPROPYL BIGUANIDE (UNII: DT9D8Z79ET)  
    ASCORBYL PALMITATE (UNII: QN83US2B0N)  
    MENTHOL (UNII: L7T10EIP3A)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83062-032-2950 mL in 1 PACKET; Type 0: Not a Combination Product10/15/202310/16/2023
    2NDC:83062-032-786 mL in 1 PACKET; Type 0: Not a Combination Product10/15/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)10/15/2023
    Labeler - IIMED MEDICAL MEXICANA S DE RL DE CV (812894376)
    Establishment
    NameAddressID/FEIBusiness Operations
    IIMED MEDICAL MEXICANA S DE RL DE CV812894376repack(83062-032) , relabel(83062-032)
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