Active Ingredient
Witch hazel 86%
Witch Hazel Liquid
FDA Label NDC 49580-0390
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by P & L Development, Llc for the product Witch Hazel (NDC 49580-0390). 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 the 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
Principal Display Panel
Distilled extract of
Witch Hazel
Astringent
alcohol 14% by volume
Manufactured by:
PL Developments
1874 Hwy 72 W
Clinton, SC 29325
Questions or comments?
Call 1-877-753-3935 Monday-Friday 9AM-5PM EST
TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL AROUND OR UNDER CAP IS BROKEN OR MISSING.
FL OZ(mL
Package Label
ReadyInCase Witch Hazel Liquid
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