Label: CHAIN DRUG MARKETING ASSOCIATION, INC.- isopropyl alcohol cloth

  • NDC Code(s): 83324-305-01
  • Packager: Chain Drug Marketing Association Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 21, 2024

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

  • Active ingredient

    Isopropyl alcohol, 70% v/v

  • Purpose

    First aid antiseptic

  • Uses

    • first aid to help prevent the risk of infection in minor cuts, scrapes, and burns
  • Warnings

    For external use only.

    Flammable, keep away from fire or flame.

    When using this product

    • do not get in the eyes or apply over large areas of the body
    • in case of deep or puncture wounds, animal bites or serious burns, consult a doctor
    • do not use longer than 1 week unless directed by a doctor

    Stop use and ask a doctor

    if the condition persists or gets worse

    Keep out of reach of children.

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

  • Directions

    • clean the affected area
    • discard after a single use
    • may be covered with a sterile bandage
  • Other information

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

    water

  • Manufacturing Information

    Distributed by:
    C.D.M.A., Inc.©

    43157 W 9 Mile Rd, Novi, MI 48375 USA

    www.qualitychoice.com

    248-449-9300

    Packaged in China

    Products of Taiwan

    REF: CDMA1001V2

    V2 RE24LPD

  • Package Label

    Packet V1 RK23LPD

    Box V2 RE24LPD

  • INGREDIENTS AND APPEARANCE
    CHAIN DRUG MARKETING ASSOCIATION, INC. 
    isopropyl alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83324-305
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83324-305-01100 in 1 BOX05/01/2024
    11 in 1 PACKET
    15 mL in 1 APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00305/01/2024
    Labeler - Chain Drug Marketing Association Inc. (011920774)
    Registrant - Medline Industries, LP (025460908)