Witch Hazel Liquid
FDA Label NDC 21130-822

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Better Living Brands, Llc for the product Witch Hazel (NDC 21130-822). 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 ingredients, 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 Ingredients

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

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

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

Principal Display Panel

NDC 21130-822-43

Signature Care

Quality Guaranteed

Witch Hazel U.S.P.

Astringent

Relief of minor skin Irritations:

  • Insect bites
  • Minor cuts
  • Minor scrapes

    • Compare to T.N. Dickinson's Witch Hazel active ingredient

    16 FL OZ (1 PT) 473 mL

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    Image Description (Mm3)

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