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

Drug Label Information

Updated December 11, 2024

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

  • 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 Product01/29/202111/30/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01501/29/2021
    Labeler - Medical Products Laboratories, Inc. (002290302)