Active Ingredient
Witch hazel, USP 86%
Witch Hazel Liquid
FDA Label NDC 70000-0615
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Cardinal Health (leader) 70000 for the product Witch Hazel (NDC 70000-0615). 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, warnings, when using this product, stop use and ask a doctor if, if pregnant or breast-feeding,, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Astringent
Uses
- for relief of minor skin irritations due to:
- insect bites
- minor cuts
- minor scrapes
Warnings
For external use only.
- Avoid swallowing.
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
If Pregnant Or Breast-Feeding,
ask a health professional before use.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away..
Directions
apply to the affected area as often as necessary.
Other Information
- keep tightly closed
- store at room temperature
Inactive Ingredient
alcohol 14% by volume
Questions Or Comments?
Call 1-877-753-3935 Monday-Friday 9AM-5PM EST
Principal Display Panel
Witch Hazel
USP, 86% | Astringent
Alcohol 14% by Volume
For relief of Minor Skin Irritations Due To
Insect Bites
Minor Cuts
Minor Scrapes
FL OZ (mL)
TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING.
DIST. BY
CAH DUBLIN, OH 43017
www.myleader.com
Package Label
LEADER Witch Hazel
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