FDA.reportPublic FDA data

SKIN TONER

Manufacturer
Universal Distribution Center LLC
Effective date
2020-12-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:36:25

Label at a glance#

ProductSKIN TONER
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

Aqua, Ethyl Alcohol, Aloe Barbadensis (Aloe Vera) Leaf Juice, Parfum

SPL UNCLASSIFIED SECTION

WITH ALOE VERA

SKIN CLEANSER

MAKE-UP REMOVER

AFTER SHAVING

For Face & Body

Clean | Soothe | Treat

Gentle Relief For 

Greasy, Rough, Injured, Inflamed, or Blemished Skin

NATURAL 100% 

WITH WITCH HAZEL (HAMAMEUS WATER)

Specifically formulated for purifying and conditioning of the skin.

Distributed by:

Universal Distribution Centre LLC

Edison, NJ 08817

www.universaldc.com

Made in Pakistan

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

UToner1UToner1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52000-300-022022-07-29C16284748780-1e4f33bdf-b196-d8a0-e053-dadaa90a6e4eSKIN TONER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52000-300-02SKIN TONER473 mL in 1 BOTTLELIQUID4731

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52000-300SKIN TONER (WITCH HAZEL) LIQUID [UNIVERSAL DISTRIBUTION CENTER LLC]1Legacy NDC, 1 package rows20210105_b2ddc67d-c4bb-4227-af88-75c08135074b.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52000-30052000-300-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
WITCH HAZEL101I4J0U34ACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT
ALOE VERA LEAFZY81Z83H0XIACT

Source Document#

Source XML

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
01a8151a-436b-4638-aef0-c682117c5aaeb2ddc67d-c4bb-4227-af88-75c08135074b2020-12-29WarningsExact identifier
spl id: 01a8151a-436b-4638-aef0-c682117c5aae
spl set id: b2ddc67d-c4bb-4227-af88-75c08135074b

Reported adverse events (FAERS/openFDA)#

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