Label: HEALTH MART WITCH HAZEL- witch hazel liquid

  • NDC Code(s): 62011-0268-1
  • Packager: Strategic Sourcing Services LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph 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 March 17, 2022

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Witch Hazel

  • Purpose

    Astringent

  • Indications

    For relief of minor skin Irritations due to

    minor cuts

    minor scraps

    insect bites

  • Warnings

    For external use only

    avoid contact with eyes

    If contact occurs rinse thoroughly with water.

  • When using this product stop using and contact a doctor if

    condition persists or gets worse

    symptoms do not improve within 7 days

  • Keep out of reach of children.

    In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

    In case of eye contact flush eyes with running water for 15 minutes.

  • Directions

    Apply liberally to the afflicted area as often as necessary

  • Inactive ingredients

    Alcohol 14% and purified water.

  • New label

    HMWitch.jpgNew

  • INGREDIENTS AND APPEARANCE
    HEALTH MART WITCH HAZEL 
    witch hazel liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62011-0268
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL855 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62011-0268-1473 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34701/01/2016
    Labeler - Strategic Sourcing Services LLC (116956644)
    Registrant - Pharma Nobis, LLC (118564114)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pharma Nobis, LLC118564114manufacture(62011-0268) , analysis(62011-0268) , pack(62011-0268) , label(62011-0268)