Witch Hazel

Manufacturer: Wal-Mart Stores, Inc. | Vi-Jon, LLC
Effective date: 2023-03-06
Label type: HUMAN OTC DRUG LABEL
Version: 7
Source: legacy-cache
Hydrated at: 2026-08-01 21:34:54

Label at a glance#

ProductWitch Hazel

Active ingredientWITCH HAZEL

Label structure7 sections

Dosage and administration

apply as often as needed

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Witch hazel 86%

Purpose

OTC - PURPOSE SECTION

Astringent

Use

INDICATIONS & USAGE SECTION

for relief of minor skin irritations due to:
•insect bites • minor cuts •minor 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 worsens or symptoms persists 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 ingredient

INACTIVE INGREDIENT SECTION

alcohol 14% by volume

adverse reactons

ADVERSE REACTIONS SECTION

This product is not manufactured or distributed by Dickinson Brands, Inc., owner of the registered trademark T.N. Dickinson's

DISTRIBUTED BY: Walmart, Inc., Bentonville, AR 72716

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 49035-633-43

equate

Compare to T.N. Dickinson Witch Hazel Active ingredient

Witch

Hazel

USP

Astringent

Made in the UJSA Factory Certified

Empty & Replace Cap

PLASTIC BOTTLE

how2recycle.info

16 FL OZ (1PT) 473 mL

image description

Products#

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

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

Witch Hazel
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
49035-653	49035-653-43

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
Name	UNII	Kind
WITCH HAZEL	101I4J0U34	ACTIB
ALCOHOL	3K9958V90M	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
24885eee-4456-9c77-e063-6394a90a485e			e3963bbb-e192-45a5-9920-650add361ca8	2024-10-15	Warnings, Adverse reactions	Exact identifier spl set id: e3963bbb-e192-45a5-9920-650add361ca8

Reported adverse events (FAERS/openFDA)#

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