FDA.reportPublic FDA data

Universal WITCH HAZEL - Universal Distribution Center LLC

Manufacturer
Universal Distribution Center LLC
Effective date
2026-07-22
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
daily-update
Hydrated at
2026-07-31 05:10:28

Label at a glance#

ProductUniversal WITCH HAZEL
Active ingredientWITCH HAZEL
Label structure8 sections

Label contents#

Full prescribing information#

Active Ingredients:

OTC - ACTIVE INGREDIENT SECTION

All natural distilled witch hazel 100%
(contains natural grain alcohol 14%)

Purpose

OTC - PURPOSE SECTION

Astringent

Usage:

INDICATIONS & USAGE SECTION

The soft toner is specifically developed to meet ultimate needs of purifying and conditioning for an array of skin types. It is a calm and non-drying formula which removes remaining traces of soap. It removes make-up or excess oils making your skin feeling soft, healthful, and smooth. It also smoothens the skin after shaving. Use as often as necessary. Apply directly from the bottle or dampen a cotton pad and smoothly wipe it off.

Warning:

WARNINGS SECTION

For external use only. Avoid contact with eyes. If contact occurs, flush thoroughly with water.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Direction:

DOSAGE & ADMINISTRATION SECTION

• remove protective inner seal
• moisten cotton ball or cleansing pad and gently wipe skin
• apply as often as necessary

Ingredients:

INACTIVE INGREDIENT SECTION

Water, Hamamelis Virginiana (Witch Hazel) Leaf Water, Alcohol (14% by Volume), Benzyl Alcohol, Methylchloroisothiazolinone, methylisothiazolinone.

SPL UNCLASSIFIED SECTION

SKIN CLEANSER

MAKE-UP REMOVER

AFTER SHAVING

For Face & Body

Clean | Soothe | Treat

Gentle Relief For
Greasy, Rough,
Injured,
Inflamed, or
Blemished Skin

100% NATURAL ASTRINGENT

Specifically formulated for purifying and conditioning of the skin.

Mfd for and Distributed By:
Universal Distribution Center LLC
330 Applegarth Road,
Monroe Township, NJ 08831

www.universaldc.com

Made in Jordan

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

witchhazel-1witchhazel-1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130676979556055GTIN-13: 0676979556055
EAN-13: 0676979556055
GTIN-12: 676979556055
UPC-A: 676979556055
GTIN storage (14 digits): 00676979556055		52000414-5.jpg

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52000-41452000-414-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
WITCH HAZEL101I4J0U34ACTIB
WATER059QF0KO0RIACT
HAMAMELIS VIRGINIANA LEAF WATER8FP93ED6H2IACT
ALCOHOL3K9958V90MIACT
BENZYL ALCOHOLLKG8494WBHIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22024-12-12full-release2026-06-01 00:43:19

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
Universal WITCH HAZELWITCH HAZELUniversal Distribution Center LLC7e0b56ef-fa41-4862-b387-5b58d81d67d42026-07-22WarningsExact identifier
ndc (package): 52000-414-06
ndc (product): 52000-414
ndc11 (package): 52000041406
spl id: c450c3e1-82b3-4bec-bc04-0d11fae30657
spl set id: 7e0b56ef-fa41-4862-b387-5b58d81d67d4

Reported adverse events (FAERS/openFDA)#

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