Witch Hazel Liquid
FDA Label NDC 37808-822

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by H E B for the product Witch Hazel (NDC 37808-822). 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

REMOVE STICKER ON PUMP PRIOR TO USE.  (FOR PUMP BOTTLES)

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

For Pump

remove sticker prior to use.  Pump onto a clean pad and apply as often as needed.

Inactive Ingredient

alcohol 14% by volume

Adverse Reaction

MADE WITH PRIDE  & CARE FOR

H-E-B, SAN ANTONIO, TX 78204

Principal Display Panel

PUSH PUMP

H-E-B

Witch Hazel U.S.P.

Astringent

  • Cleans & Refreshes
  • For Relief of Minor Skin Irritations due to Insects Bites, Minor Cuts and Minor Scrapes

    • 8 FL OZ (236 mL)

    Image Description (Mm01)

    Image Description (Mm01)

* Please review the disclaimer below.