Witch Hazel

Manufacturer
Liberty Procurement, Inc | Consumer Product Partners, LLC
Effective date
2024-07-31
Label type
HUMAN OTC DRUG LABEL
Version
16
Source
legacy-cache
Hydrated at
2026-08-01 20:57:32

Label at a glance#

ProductWitch Hazel
Active ingredientWITCH HAZEL
Label structure11 sections

Dosage and administration

apply as often as needed

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Witch Hazel 86%

Purpose

OTC - PURPOSE SECTION

Astringent

Use

INDICATIONS & USAGE SECTION

for relief of minor skin irritations due to:

  • insects bites
  • minor cuts
  • monor scrapes

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

  • avoid contact with the eyes.  If contact occurs, rinse thoroughly with water

stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worses or symptoms last for more than 7 days

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

apply as often as needed

Inactive ingredients

INACTIVE INGREDIENT SECTION

alcohol 14% by volume

SPL UNCLASSIFIED SECTION

Distributed by

Liberty Procurement, Inc

650 Liberty Ave.

Union, NJ 07083 USA

Visit us at: www. facevalues.com

SATIDFACTION GUARANTEED

Or Your Money Back

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

COREVLAUES

Witch Hazel USP

  • Astringent - Cleans & refreshes face & body; Gentle, non-drying
  • Soothes & relieves minor skin irritations - Treats insect bites, minor cuts & scrapes

16 FL OZ (1 PT) 473 mL

image descriptionimage description

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63940-822WITCH HAZEL LIQUID [LIBERTY PROCUREMENT, INC]16Legacy NDC20240802_a8fa4214-1938-4cfb-8321-4b0249e2474e.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63940-82263940-822-43

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
WITCH HAZEL101I4J0U34ACTIB

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
37b6230f-6d34-bcce-e063-6294a90a3b18a8fa4214-1938-4cfb-8321-4b0249e2474e2025-06-16WarningsExact identifier
spl set id: a8fa4214-1938-4cfb-8321-4b0249e2474e

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.