Label: EAGLE WIPES HAND SANITIZING WIPES WITH ALOE VERA- benzalkonium chloride 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 January 12, 2023

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  • OTC - Purpose

    antimicrobial

  • Warnings

    For External Use only.

    Do not use In eyes.

    Do not use if you are allergic to any of the ingredients.

    When using this product if eye contact occurs, rinse eves thoroughlv with water.

    Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours.

  • OTC - Do not use

    In eyes

    If you are allergic to any of the ingredients.

  • OTC - Keep out of reach of children.

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

  • Dosage and administration

    Directions:

    To Begin:

    Make a small cut along top of refill pouch to open and expose wipes. Keep wipes in pouch. Pinch center wipe from pouch and pull up through wipe dispenser opening. Place entire pouch into dispenser and close.

    For use:

    Gently pull wipe(s) from dispenser feed. Dispose wipe after each use. DO NOT FLUSH.

  • OTC - Active Ingredient

    Benzalkonium Chloride

  • Inactive Ingredients

    Sodium chloride

    Citric acid monohydrate

    Water

    Sodium acetate

    Benzyl alcohol

    Sodium Hydroxymethylglycinate

    Aloe Vera Leaf

    Potassium Sorbate

  • Indications & Usage

    Antibacterial

    For hand washing to decrease bacteria on the skin. May be used on hands.

  • Package label, principal display paneel

    Eagle Wipes Hand Sanitizing Wipes with Aloe VeraAloe Vera Sanitizing Wipes

  • INGREDIENTS AND APPEARANCE
    EAGLE WIPES HAND SANITIZING WIPES WITH ALOE VERA 
    benzalkonium chloride swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76801-972
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.0013 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    WATER (UNII: 059QF0KO0R)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    SODIUM HYDROXYMETHYLGLYCINATE (UNII: DIG6BWZ9XT)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76801-972-80100 g in 1 PACKAGE; Type 0: Not a Combination Product04/28/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/28/2020
    Labeler - TEXAS RAGTIME INC (007677040)
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