Witch Hazel Liquid
FDA Label NDC 71990-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Arcadia Beauty Labs Llc for the product Witch Hazel (NDC 71990-001). 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: relieves minor skin irritation due to:, 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.

Active Ingredient

Witch Hazel 86%

Purpose

Astringent

Uses: Relieves Minor Skin Irritation Due To:

  • insect bites
  • minor cuts
  • minor scrapes

Warnings

For external use only

When Using This Product

  • Avoid contact with 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

  • After cleansing apply generously to cotton ball and gently wipe skin.
  • Apply as often as needed.

Inactive Ingredients

Alcohol 14% by volume.

Principal Display Panel

BEYOND BELIEF

Skin Renewing Witch Hazel

FACIAL ASTRINGENT

REFRESH - SKIN RENEWAL

Gently cleanses and

tones to leave skin

soft and refreshed

Image Description (Witchhazel)

Image Description (Witchhazel)

473 mL 16 fl oz.

Image Description (Witchhazel)

Image Description (Witchhazel)

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