Label: PHARMACIST CHOICE ALCOHOL PREP PADS- isopropyl alcohol swab

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated October 18, 2022

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  • Active Ingredients

    Isopropyl Alcohol USP, 70% v/v

  • Purpose

    Antiseptic

  • Keep out of children

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

  • Use

    For preparation of skin prior to injection; to decrease germs in minor cuts and scrapes.

  • Warning

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

  • Directions

    Wipe injection site vigorously.

  • Inactive ingredients

    Water

  • Drug Facts

    Active Ingredients

    Isopropyl Alcohol USP, 70% v/v

    Purpose:

    Antiseptic

    Use: For preparation of skin prior to injection; to decrease germs in minor cuts and scrapes.

    Warning: For external use only. Flammable, keep away from fire and flame.

    Keep out of children.

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

    Caution: Don’t apply to a irritated skin.

    Don’t use in the eyes, or on mucous membranes.

    In case of deep or puncture wounds, consult a doctor.

    Directions: wipe injection site vigorously.

    Other information: Store at room temperature.

    Inactive ingredients: Water

    Labeling of carton

  • INGREDIENTS AND APPEARANCE
    PHARMACIST CHOICE ALCOHOL PREP PADS 
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71584-0102
    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:71584-0102-11.4 mL in 1 POUCH; Type 0: Not a Combination Product07/17/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A07/17/2017
    Labeler - Guangdong Comfort Medical Products Co., Ltd. (544507534)
    Registrant - Guangdong Comfort Medical Products Co., Ltd. (544507534)
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