Witch Hazel Solution
FDA Label NDC 41163-822

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by United Natural Foods, Inc. Dba Unfi for the product Witch Hazel (NDC 41163-822). 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, uses, 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

Uses

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 persist 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

Other

  • cleans and refreshes skin
  • tones skin
  • soothes sunburn

    • Distriubuted by SUPERVALE INC.

    Eden Praiie, MN 55344

    Contact us at 1-877-932-7948

    or www.supervalu-ourownbrands.com

Principal Display Panel

NDC 41163-822-43

EQUALINE

witch hazel

astringent

hamamelis water

for relief of minor skin

irritations due to:

  • insects bites
  • minor cuts
  • minor scrapes

    • 16 FL OZ (1 PT ) 473 mL

    Image Description (Mm1)

    Image Description (Mm1)

    822.001/822AA

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