Label: WITCH HAZEL liquid

  • NDC Code(s): 10733-801-08, 10733-801-16
  • Packager: Medical Products Laboratories, Inc.
  • 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 February 17, 2021

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  • Warnings

    For external use only

    When using this product

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

    Stop use and ask a doctor if

    • condition worsens or symptoms last for more than 7 days

    Keep out of reach of children.

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

    MANUFACTURED BY:

    MEDICAL PRODUCTS LABORATORIES, INC.

    9990 GLOBAL ROAD, PHILADELPHIA 19115

    mplusa.com

    Questions or comments? Call 1-800-523-0191

  • Witch Hazel For Face & Body

    ASTRINGENT

    Relief of minor skin irritations due to:

    • Insect bites
    • Minor cuts & scrapes

    Active ingredient

    Witch hazel 86%

    Purpose

    Astringent

    Inactive ingredient:

    alcohol 14% by volume

    Use

    for relief of minor skin irritations due to:

    • insect bites • minor cuts • minor scrapes

    Directions

    apply as often as needed

  • 10733-801-08

    10733-801-08

  • 10733-801-16

    witch hazel

  • INGREDIENTS AND APPEARANCE
    WITCH HAZEL 
    witch hazel liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10733-801
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL86 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10733-801-08236 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product01/29/2021
    2NDC:10733-801-16473 mL in 1 BOTTLE; Type 0: Not a Combination Product01/29/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34601/29/2021
    Labeler - Medical Products Laboratories, Inc. (002290302)
    Registrant - Medical Products Laboratories, Inc. (002290302)
    Establishment
    NameAddressID/FEIBusiness Operations
    Medical Products Laboratories, Inc.002290302pack(10733-801) , manufacture(10733-801) , analysis(10733-801)
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