Witch Hazel Liquid
FDA Label NDC 0363-0803

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Walgreen Co. for the product Witch Hazel (NDC 0363-0803). 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:

  • insects bites
  • minor cuts
  • monor 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 worses or symptoms last 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 Ingredients

alcohol 14% by volume

Other

*Walgreens Pharmacist survey study, November 2014.

Questions Or Comments?

1-888-593-0593

Adverse Reactions

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

DISTRIBUTED BY: WALGREEN CO.

200 WILMOT RD., DEERFIELD, IL 60015

100% SATISFACTION GUARANTEED

walgreens.com 

* Please review the disclaimer below.