Label: AER TRAVELER TOWELETTE- aer traveler solution

  • NDC Code(s): 50289-4200-1
  • Packager: Birchwood Laboratories LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 8, 2026

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  • ACTIVE INGREDIENT

    Witch Hazel 50%

  • PURPOSE

    Astringent

  • INDICATIONS & USAGE

    Temporary relief of anal itching & burning

  • WARNINGS

    For external use only

  • STOP USE

    Stop use and ask doctor if rectal bleeding or continued irritation occurs

  • ASK DOCTOR

    Stop use and ask doctor if rectal bleeding or continued irritation occurs

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • INSTRUCTIONS FOR USE

    Gently apply to affected areas by patting and then discard

  • INACTIVE INGREDIENT

    Benzalkonium Chloride, Citric Acid, Glycerin, Methylparaben, Purified Water, Sodium Citrate

  • DESCRIPTION

    PRE-MOISTENED WITCH HAZEL TOWELETTE

  • DOSAGE & ADMINISTRATION

    Gently apply to affected areas by patting and then discard

  • AER Traveler Packet Artwork

    Packet Artwork

  • INGREDIENTS AND APPEARANCE
    AER TRAVELER TOWELETTE 
    aer traveler solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50289-4200
    Route of AdministrationTOPICAL, RECTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL0.5 g
    Inactive Ingredients
    Ingredient NameStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    WATER (UNII: 059QF0KO0R)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50289-4200-150 in 1 CARTON11/07/2024
    11 in 1 PACKET
    11 in 1 APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01511/07/2024
    Labeler - Birchwood Laboratories LLC (096488432)
    Registrant - Birchwood Laboratories LLC (096488432)
    Establishment
    NameAddressID/FEIBusiness Operations
    Birchwood Laboratories LLC096488432manufacture(50289-4200)
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