Label: MEDLINE- ethyl alcohol swab

  • NDC Code(s): 53329-133-27, 53329-133-78
  • Packager: Medline Industries, LP
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 30, 2023

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

View All Sections
  • 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 fire or flame.

    Do not use

    • • in the eyes
    • • on children under 2 years of age unless directed by a doctor

    Ask a doctor before use if injuries are

    • • deep or puncture wounds
    • • serious burns

    Stop use and ask a doctor if

    • • redness, irritation, swelling or pain persists or increases
    • • infection occurs

    Keep out of reach of children.

    If accidentally swallowed, seek medical assistance or immediately contact a Poison Control Center.

  • Directions

    directions

    • 1. use a tissue to clean the inside of both nostrils, including the inside tip of nostril. Discard
    • 2. insert swab comfortably into tip of right nostril and rotate for 30 seconds, covering all surfaces
    • 3. using same swab, repeat step 2 with tip of left nostril
    • 4. do not blow nose. If solution drips, gently wipe with a tissue
  • Other information

    • • protect from freezing and avoid excessive heat
    • • not made with natural rubber latex
  • Inactive ingredients

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

  • Manufacturing Information

    Manufactured by:

    Medline Industries, LP

    Three Lakes Drive, Northfield, IL 60093 USA

    Made in USA

    1-800-MEDLINE (633-5463)

    REF: MDSR1971

    V2 RJ21APL

  • Package Label

    Label V2 RJ21APL frontLabel V2 RJ21APL back

  • INGREDIENTS AND APPEARANCE
    MEDLINE 
    ethyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53329-133
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    MENTHOL (UNII: L7T10EIP3A)  
    ASCORBYL PALMITATE (UNII: QN83US2B0N)  
    CASTOR OIL (UNII: D5340Y2I9G)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    WATER (UNII: 059QF0KO0R)  
    POLYAMINOPROPYL BIGUANIDE (UNII: DT9D8Z79ET)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53329-133-2710 in 1 BOX01/01/202201/31/2025
    1NDC:53329-133-786 mL in 1 PACKET; Type 0: Not a Combination Product
    2NDC:53329-133-786 mL in 1 PACKET; Type 0: Not a Combination Product01/01/202201/31/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)01/01/202201/31/2025
    Labeler - Medline Industries, LP (025460908)
    Registrant - Medline Industries, LP (025460908)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!