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Medi-First Plus Sterile Alcohol Pads (Unifirst First Aid Corporation)

Available Formats

Dosage Form Package Information Links
LIQUID 50 PACKET in 1 BOX (47682-931-50) > 1 PACKET in 1 PACKET > .8 mL in 1 PACKET Label Information
LIQUID 4000 PACKET in 1 CASE (47682-931-51) > 1 PACKET in 1 PACKET > .8 mL in 1 PACKET Label Information

Complete Medi-First Plus Sterile Alcohol Pads Information

  • Drug Facts


  • Active ingredient

    Isopropyl Alcohol 70% v/v



  • Purpose

    Antiseptic


  • Uses

    • for preparation of the skin prior to injection
    • first aid use to decrease germs in minor cuts, scrapes and burns

  • Warnings

    Flammable, keep away from fire or flame.

    For external use only.

    Do not use
    • with electrocautery procedures
    • in or near the eyes
    • longer than 1 week unless directed by a doctor

    In case of deep or puncture wounds, animal bites or serious burns, consult a doctor.

    Stop use and ask a doctor if
    • irritation and redness develops
    • condition persists for more than 72 hours

  • 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 or
    • apply to cut, scrape or burn and discard after single use

  • Other information

    • protect from freezing and avoid excessive heat

  • Inactive ingredient

    water


  • Questions?

    Call 1-800-634-7680


  • Medi-First Plus Alcohol Wipes Label

    Medi-First Plus® Alcohol Wipes

    Sterile

    50 Wipes

    AlcoholWipes 103150


  • INGREDIENTS AND APPEARANCE
    MEDI-FIRST PLUS STERILE ALCOHOL PADS 
    isopropyl alcohol liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:47682-931
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:47682-931-50 50 in 1 BOX 12/23/2011
    1 0.8 mL in 1 PACKET; Type 0: Not a Combination Product
    2 NDC:47682-931-51 4000 in 1 CASE 12/23/2011 08/16/2017
    2 0.8 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 12/23/2011
    Labeler - Unifirst First Aid Corporation (832947092)
    Establishment
    Name Address ID/FEI Business Operations
    Phoenix Innovative Healthcare Manufacturers 650687176 manufacture(47682-931)