Label: PROGRESS ANTIBACTERIAL WIPES LEMON SCENT- benzalkonium chloride cloth

  • 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 November 25, 2020

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  • Drug Facts

  • Active Ingredient

    Benzalkonium chloride 0.13%

    Purpose

    Antiseptic

  • Uses

    • For hand sanitizing to decrease bacteria on the skin.
    • Apply topically to the skin to help prevent cross contamination.
    • Recommended for repeated use.
    • Dries in seconds.
  • Warnings

    For external use only.

    When using this product

    do not use in or contact the eyes.

    Stop use and ask a doctor is

    too much skin irritation or sensitivity develops or increases.

    Keep this out of reach of children.

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

  • Directions

    • Gently pull back resealable label, remove and use wipe as required.
    • Reseal back after use.
  • Other information

    • Lot No. Manufacture date and Expiration date can be found on package.
  • Inactive Ingredients

    Water, Phenoxyethanol, DMDM Hydantoin, Polysorbate 20, Ethylparaben, Methylparaben, Disodium Citrate, Aloe Barbadensis Leaf Juice, Parfum

  • Package Labeling:

    Bottle

  • INGREDIENTS AND APPEARANCE
    PROGRESS ANTIBACTERIAL WIPES LEMON SCENT 
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80882-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    ETHYLPARABEN (UNII: 14255EXE39)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    DISODIUM HYDROGEN CITRATE (UNII: 6FO62KCQ7A)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80882-002-5050 in 1 BAG11/20/2020
    14.04 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E11/20/2020
    Labeler - Truechoicepack, Corp (078786060)
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