Sunmark Witch Hazel

Manufacturer: Strategic Sourcing Services LLC | Pharma Nobis, LLC
Effective date: 2023-12-19
Label type: HUMAN OTC DRUG LABEL
Version: 6
Source: full-release
Hydrated at: 2026-06-01 00:04:53

Label at a glance#

ProductSunmark Witch Hazel

Active ingredientWITCH HAZEL

Label structure10 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.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SMWitch.jpgNDC 49348-181-38

witch

hazel

A lcohol 14%

16 FLOZ (1 PT) 473 mL

Principal Display Panel NDC 49348-181-38 witch hazel Alcohol 14% 16 FL OZ (1 PT) 473 mL

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
7792dadb-52b6-46b6-8fdf-80b1171065b5	Product name	1	20180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
49348-181-38	Sunmark Witch Hazel	473 mL in 1 BOTTLE	LIQUID	473		6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49348-181	SUNMARK WITCH HAZEL (WITCH HAZEL) LIQUID [STRATEGIC SOURCING SERVICES LLC]	6	Current NDC, Legacy NDC, 1 package rows	20231220_08c00c1a-7ec8-4624-9db0-a0e8430cd126.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
49348-181-38	ML - Milliliter	49348-181	e2ea7e38-a952-4ffc-a6d4-9f3236ecf858	1	2023-08-08

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Sunmark Witch Hazel
Witch Hazel
ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
49348-181	49348-181-38

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
Sunmark Witch Hazel	WITCH HAZEL	Strategic Sourcing Services LLC	08c00c1a-7ec8-4624-9db0-a0e8430cd126	2023-12-19	Warnings	Exact identifier ndc (package): 49348-181-38 ndc (product): 49348-181 ndc11 (package): 49348018138 spl id: 0ce5bdec-f4fd-73d9-e063-6294a90a6a87 spl set id: 08c00c1a-7ec8-4624-9db0-a0e8430cd126

Reported adverse events (FAERS/openFDA)#

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