Otc - Active Ingredient
Witch Hazel 100% (Containing alcohol 14% by Volume)
Witch Hazel Liquid
FDA Label NDC 69842-330
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Cvs Health for the product Witch Hazel (NDC 69842-330). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - when using, otc - ask doctor, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Astringent
Indications & Usage
Use for relief of minor skin irritations due to
- Insect bites
- minor cuts
- minor scrapes
Warnings
For External use only
Otc - When Using
Avoid contact with eyes. If contact occurs, rinse thoroughly with water
Otc - Ask Doctor
Stop use and ask a doctor if
- condition worsens or symptoms last for more than 7 days
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control right away
Dosage & Administration
Apply as often as needed
Inactive Ingredient
Alcohol
* Please review the disclaimer below.
