Witch Hazel

Manufacturer: Humco Holding Group, Inc.
Effective date: 2020-06-20
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 23:18:28

Label at a glance#

ProductWitch Hazel

Active ingredientWITCH HAZEL

Label structure12 sections

Dosage and administration

Apply liberally to the afflicted area as often as necessary

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Witch Hazel

Purpose

OTC - PURPOSE SECTION

Astringent

Indications

INDICATIONS & USAGE SECTION

For relief of minor skin Irritations due to

minor cuts

minor scraps

insect bites

Warnings

WARNINGS SECTION

For external use only

avoid contact with eyes

If contact occurs rinse thoroughly with water.

When using this product stop using and contact a doctor if

OTC - STOP USE SECTION

condition persists or gets worse

symptoms do not improve within 7 days

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

In case of eye contact flush eyes with running water for 15 minutes.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply liberally to the afflicted area as often as necessary

Inactive ingredients

INACTIVE INGREDIENT SECTION

Alcohol 14% and purified water.

Good Neighbor Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display Panel NDC 46122-335-43 Witch Hazel (Hamamelis Water) Distilled Extract Alcohol 14% by volume 16 fl oz (1 pt) 473 mL

Sunmark Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Health Mart Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HMWitch.jpjHM

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
0395-9125-16	2022-07-29	C162847	48780-1	e4f33bdf-a079-d8a0-e053-dadaa90a6e4e	Private Label Witch Hazel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0395-9125-16	Witch Hazel	473 mL in 1 BOTTLE	LIQUID	473		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0395-9125	WITCH HAZEL LIQUID [HUMCO HOLDING GROUP, INC.]	3	Legacy NDC, 1 package rows	20200622_606553b1-054a-15a7-e053-2a91aa0ad05b.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

Witch Hazel
ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
0395-9125	0395-9125-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	IACT
WATER	059QF0KO0R	IACT
WITCH HAZEL	101I4J0U34	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
a885bf6f-9e5e-ee9e-e053-2a95a90a35b7			606553b1-054a-15a7-e053-2a91aa0ad05b	2020-06-20	Warnings	Exact identifier spl id: a885bf6f-9e5e-ee9e-e053-2a95a90a35b7 spl set id: 606553b1-054a-15a7-e053-2a91aa0ad05b

Reported adverse events (FAERS/openFDA)#

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