Witch Hazel Solution
FDA Label NDC 63868-592

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Chain Drug Marketing Association Inc for the product Witch Hazel (NDC 63868-592). 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, stop use and ask a doctor if, otc - keep out of reach of children, directions, inactive ingredients, principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient                                     Purpose

Witch hazel ................................................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 eyes

Stop Use And Ask A Doctor If

  • condition worsens or symptoms persist for more than 7 days

Otc - Keep Out Of Reach Of Children

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 Ingredients

alcohol and purified water

Principal Display Panel

Image Description (Label2)

Image Description (Label2)

Image Description (Label1)

Image Description (Label1)

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