Label: ANTISEPTIC CLEANSING WIPES- chlorhexidine gluconate swab

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated October 18, 2022

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  • Active ingredient

    Chlorhexidine Gluconate 0.02%

  • Purpose

    Antiseptic

  • CAUTION: Keep out of reach of children

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

  • Use

    Antiseptic cleansing of the desired area.

  • Warnings

    For external use only. Flammable, keep away from fire or flame.

    Do not use

    in the eyes.

    Stop use

    If irritation, redness or other symptoms develop.

    Ask a doctor

    If condition persists or gets worse.

  • Directions

    Tear open packet, unfold towelette, and use to cleanse desired skin area.

  • Inactive ingredients

    Purified water, 0.5% R-CO2Na, 0.2% Cetrimide

  • DRUG FACTS

    Active ingredient

    Chlorhexidine Gluconate 0.02%

    Purpose

    Antiseptic

    Use

    Antiseptic cleansing of the desired area.

    Warnings

    For external use only.

    Do notuse

    ﹒in the eyes.

    Stop use

    If irritation, redness or other symptoms develop.

    Ask a doctor

    If condition persists or gets worse.

    CAUTION: Keep out of reach of children.

    If swallowed, get medical help right away.

    Directions

    Tear open packet, unfold towelette, and use to cleanse desired skin area.

    Other information: Store at room temperature.

    Inactive ingredients

    Purified water, 0.5% R-CO 2Na, 0.2% Cetrimide

    image of carton labeling

    image of packet labeling

  • INGREDIENTS AND APPEARANCE
    ANTISEPTIC CLEANSING WIPES 
    chlorhexidine gluconate swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71584-0106
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE GLUCONATE0.0002 mg  in 1 mg
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CETRIMIDE (UNII: 24QSH2NL8N)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71584-0106-11.2 mg in 1 PACKET; Type 0: Not a Combination Product07/17/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/17/2017
    Labeler - Guangdong Comfort Medical Products Co., Ltd. (544507534)
    Registrant - Guangdong Comfort Medical Products Co., Ltd. (544507534)