Witch Hazel Liquid
FDA Label NDC 59779-045

12 label sections · Submitted to the FDA by Cvs Pharmacy, Inc. · Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Cvs Pharmacy, Inc. for the product Witch Hazel (NDC 59779-045). 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 100% (containing alcohol 14% by volume)

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

None

Disclaimer

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

Adverse Reaction

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Pat. D675, 101

Principal Display Panel

NDC 59779-045-43

CVS ™

WITCH HAZEL

Astringent for Face & Body

Compare to T.N. Dickinson's Witch Hazel ®*

Relief of minor skin irrations due to:

Insect bites, Minor cuts & scrapes

16 FL OZ (1 PT) 473 mL

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* Please review the disclaimer below.