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Drug Facts
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HYDROX LABORATORIES
825-B Tollgate Rd.• Elgin, IL 60123
Witch Hazel Liquid
FDA Label NDC 10565-040
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hydrox Laboratories for the product Witch Hazel (NDC 10565-040). 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 other, active ingredient, purpose, uses, warnings, keep out of reach of children, directions, otc - stop use, 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
Uses
For relief of minor skin irritations due to insect bites, minor cuts, minor scrapes.
Warnings
FOR EXTERNAL USE ONLY.
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Apply to the affected area as often as necessary. When using this product, avoid contact with the eyes.
Otc - Stop Use
Stop use and ask a doctor if Condition worsens or symptoms persist for more than 7 days.
Inactive Ingredient
Alcohol 14% by volume
Principal Display Panel - 473 Ml Bottle Label
Personal Care
FreshMoment
Witch Hazel
Natural Astringent
Cleans and Refreshes Skin
No Artificial Fragrance
or Dyes
MADE IN USA
16 FL. OZ. (473mL)
Principal Display Panel (473 mL Bottle Label)
* Please review the disclaimer below.
