WITCH HAZEL LIQUID [DOLGENCORP, LLC]

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WITCH HAZEL LIQUID [DOLGENCORP, LLC]
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NDC 55910-822-43
Set ID 5d5b4cd3-a485-4a27-8771-d200edb0fa61
Category HUMAN OTC DRUG LABEL
Packager OLD EAST MAIN CO.
Generic Name
Product Class
Product Number
Application Number PART347
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  • Active ingredient

    Witch hazel 86%

  • Purpose

    Astringent

  • Uses

    For relief of minor skin irritations due to:

    • insect bites
    • minor cuts
    • minor scrapes
  • Warnings

    For external use only

  • When using this prodct

    avoid contact with the eyes.  If contact occurs, rinse thoroughly with water.

  • Stop use and ask a doctor if

    condition worsens or symptoms persis for more than 7 days

  • Keep out of reach of children

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

  • Directions

    apply as often as needed

  • Inactive ingredient

    alcohol 14% by volume

  • adverse reaction

    DISTRIBUTED BY ONE EAST MAIN CO

    100 MISSION RIDGE

    GOODLETTSVILLE, TN 37072

    100%    Satisfaction Guaratneed

  • principal display panel

    DG| health

    Witch

    Hazel USP

    Astringent

    For relief of minor skin irritations due to:

    • Insect Bites
    • Minor Cuts
    • Minor Scraped

    100% Satisfaction Guaranteed! (888)309-9030

    16 FL OZ (1 PT) 473 mL

    image description

  • principal display panel

    Since 1903

    Rexall

    Witch

    Hazel

    Astringent

    For relief of minor skin irritations due to:

    • Insects bites
    • Minor cuts
    • Minor scrapes

    16 FL OZ (1PT) 473mL

    image description

  • INGREDIENTS AND APPEARANCE
    WITCH HAZEL 
    witch hazel liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55910-822
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL979 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55910-822-43473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/05/1989
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34707/05/1989
    Labeler - OLD EAST MAIN CO. (068331990)
    Registrant - Vi Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi Jon, LLC790752542manufacture(55910-822)
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