Witch Hazel Liquid
FDA Label NDC 56062-822

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Publix Super Markets, Inc. for the product Witch Hazel (NDC 56062-822). 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:

  • 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

Distributed by Publix Supermarkets, Inc.

3300 Publix Corporate Parkway

Lakeland, FL 33811 publix.com

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

Pat. Pend

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Publix

Distilled Extract Witch Hazel

Alcohol 14%

Astringent

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

Compare to TN Dickinson's Witch Hazel

16 FL OZ (1 PT) 473 mL

Image Description (Mm02)

Image Description (Mm02)

* Please review the disclaimer below.