Label: ALCOHOL swab

  • NDC Code(s): 68786-300-01, 68786-300-02
  • Packager: Sion Biotext Medical Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 24, 2024

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

  • Active Ingredient

    Isopropyl Alcohol 70% v/v

  • Purpose

    Antiseptic

  • Uses

    First aid to help prevent infection in minor cuts, scrapes and burns

    For preparation of the skin prior to an injection

  • Warnings

    • For external use only
    • Flammable, keep away from flame or fire
  • Do not use

    • in the eyes or over large areas of the body
    • longer than 1 week unless directed by doctor
    • with electrocautery procedures
  • Ask a doctor before use if you have

    deep or puncture wounds, animal bites or serious burns

  • Stop use an ask a doctor if

    conditions persists for more than 72 hours or gets worse

  • Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions:

    • When used for first aid: Clean the affected area. Apply a small amount of this product on the area 1 to 3 times daily. May be covered with a sterile bandage. If bandaged, let dry first.
    • When used to prepare an injection site: Apply product to the injection site prior to injection.
  • Other Information:

    • Store at room temperature
    • Avoid excessive heat
  • Inactive Ingredient

    Water

  • Principal Display Panel

    NDC 68786-300-01

    4'' saturated

    50 individual packs

    Label

    NDC 68786-300-02

    4" saturated

    3 per packet

    25 packet

    Label 1

  • INGREDIENTS AND APPEARANCE
    ALCOHOL 
    alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68786-300
    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:68786-300-0110 in 1 CASE10/09/2020
    150 in 1 BOX
    11 in 1 POUCH
    11.4 mL in 1 PATCH; Type 0: Not a Combination Product
    2NDC:68786-300-0210 in 1 CASE10/09/2020
    275 in 1 BOX
    23 in 1 POUCH
    21.4 mL in 1 PATCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00310/09/2020
    Labeler - Sion Biotext Medical Ltd (532775194)
    Registrant - Sion Biotext Mexico SAPI de CV (951575186)