Warnings
For external use only
Witch Hazel Liquid
FDA Label NDC 10733-801
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Medical Products Laboratories, Inc. for the product Witch Hazel (NDC 10733-801). 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 warnings, when using this product, stop use and ask a doctor if, keep out of reach of children., manufactured by:, witch hazel for face & body, active ingredient, purpose, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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 last for more than 7 days
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Posion Control Center right away.
Manufactured By:
MEDICAL PRODUCTS LABORATORIES, INC.
9990 GLOBAL ROAD, PHILADELPHIA 19115
mplusa.com
Questions or comments? Call 1-800-523-0191
Witch Hazel For Face & Body
ASTRINGENT
Relief of minor skin irritations due to:
- Insect bites
- Minor cuts & scrapes
Active Ingredient
Witch hazel 86%
Purpose
Astringent
Inactive Ingredient:
alcohol 14% by volume
Use
for relief of minor skin irritations due to:
• insect bites • minor cuts • minor scrapes
Directions
apply as often as needed
* Please review the disclaimer below.
