Witch Hazel

Manufacturer: Family Dollar (FAMILY WELLNESS)
Effective date: 2025-02-06
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: full-release
Hydrated at: 2026-06-01 00:54:39

Label at a glance#

ProductWitch Hazel

Active ingredientWITCH HAZEL

Label structure9 sections

Indications and uses

for relief of minor skin irritations due to: insect bites minor cuts minor scrapes

Dosage and administration

apply to the affected area as often as necessary.

Contacts and useful links#

PhonePoison Help1-800-222-1222

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Witch hazel 86%

Purpose

OTC - PURPOSE SECTION

Astringent

Uses

INDICATIONS & USAGE SECTION

for relief of minor skin irritations due to:
- insect bites
- minor cuts
- minor scrapes

Warnings

WARNINGS SECTION

for external use only
avoid swallowing

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition worsens or symptoms persist for more than 7 days.

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

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 (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

apply to the affected area as often as necessary.

Other information

SPL UNCLASSIFIED SECTION

keep tightly closed
store at room temperature

Inactive ingredient

INACTIVE INGREDIENT SECTION

alcohol 14% by volume

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Modesa

ASTRINGENT

WITCH HAZEL

For Face and Body

SOOTHES MINOR SKIN IRRITATIONS

ALCOHOL 14% BY VOLUME

FL OZ (mL)

TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING.

DISTRIBUTED BY: MIDWOOD BRANDS, LLC

10611 MONROE RD, MATTHEWS, NC 28105

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
55319-590-16	2022-12-07	C162847	48780-1	d6a99b39-9f73-a426-e053-dadaa90af4c2	Drug Facts
55319-590-16	2022-01-28	C162847	48780-1	d6a99b39-9f73-a426-e053-dadaa90af4c2	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
55319-590-16	Witch Hazel	473 mL in 1 BOTTLE, PLASTIC	LIQUID	473		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
55319-590	WITCH HAZEL LIQUID [FAMILY DOLLAR (FAMILY WELLNESS)]	5	Current NDC, Legacy NDC, 1 package rows	20250209_a2047ef3-cda4-4411-a4c2-d7fb03f5b069.zip

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
55319-590	55319-590-16

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
Witch Hazel	WITCH HAZEL	Family Dollar (FAMILY WELLNESS)	a2047ef3-cda4-4411-a4c2-d7fb03f5b069	2025-02-06	Warnings	Exact identifier ndc (package): 55319-590-16 ndc (product): 55319-590 ndc11 (package): 55319059016 spl id: 91446e91-3de9-4f16-ad3c-1b93ec333162 spl set id: a2047ef3-cda4-4411-a4c2-d7fb03f5b069

Reported adverse events (FAERS/openFDA)#

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