Witch Hazel Liquid
FDA Label NDC 63941-822

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Valu Merchandisers Company for the product Witch Hazel (NDC 63941-822). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredient, purpose, use, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Witch hazel 86%

Purpose

Astringent

Use

 for relief of minor skin irritations due to:
•insect bites • minor cuts •minor scrapes

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 persists 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 Reactons

This productis not manufactured or distributed by Dickinson Brands, Inc., distributor of T. N. Dickinson's Witch Hazel.

PROUDLTY DISTRIBUTED BY: VALUE MERCHANDISERS, CO. 5000 KANSAS AVE, KANSAS CITY, KS 66106

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Witch

Hazel

U.S.P.

  • Astringent
  • For relief of minor skin irritations due to insect bites, minor cuts and scrapes
  • Cleanses, soothe, treat skin

    • 16 FL OZ (1 PT) 473 mL

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