Witch Hazel

Manufacturer: Medical Products Laboratories, Inc.
Effective date: 2024-12-11
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 00:42:32

Label at a glance#

ProductWitch Hazel

Active ingredientWITCH HAZEL

Label structure4 sections

Contacts and useful links#

PhoneLabel contact1-800-523-0191

Label contents#

Full prescribing information#

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 - ASK DOCTOR SECTION

condition worsens or symptoms last 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 Posion Control Center right away.

MANUFACTURED BY:

OTC - QUESTIONS SECTION

MEDICAL PRODUCTS LABORATORIES, INC.

9990 GLOBAL ROAD, PHILADELPHIA 19115

mplusa.com

Questions or comments? Call 1-800-523-0191

Witch Hazel For Face & Body

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ASTRINGENT

Relief of minor skin irritations due to:

Insect bites
Minor cuts & scrapes

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Witch hazel 86%

Purpose

OTC - PURPOSE SECTION

Astringent

Inactive ingredient:

INACTIVE INGREDIENT SECTION

alcohol 14% by volume

Use

INDICATIONS & USAGE SECTION

for relief of minor skin irritations due to:

• insect bites • minor cuts • minor scrapes

Directions

DOSAGE & ADMINISTRATION SECTION

apply as often as needed

10733-801-08

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

10733-801-08

10733-801-16

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

witch hazel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
200295	witch hazel 86 % Topical Solution	PSN	3
200295	witch hazel 860 MG/ML Topical Solution	SCD	3
200295	witch hazel 86 % Topical Solution	SY	3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
10733-801-08	Witch Hazel	236 mL in 1 BOTTLE, DISPENSING	LIQUID	236		3
10733-801-16	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
10733-801	WITCH HAZEL LIQUID [MEDICAL PRODUCTS LABORATORIES, INC.]	3	Current NDC, Legacy NDC, 2 package rows	20241213_b815792f-2f8f-7ac8-e053-2995a90ade18.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
10733-801	10733-801-08, 10733-801-16

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
ALCOHOL	3K9958V90M	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
Witch Hazel	WITCH HAZEL	Medical Products Laboratories, Inc.	b815792f-2f8f-7ac8-e053-2995a90ade18	2024-12-11	Warnings	Exact identifier ndc (package): 10733-801-16 ndc (package): 10733-801-08 ndc (product): 10733-801 ndc11 (package): 10733080108 ndc11 (package): 10733080116 spl id: 28dabfcb-f8d9-6b91-e063-6394a90a800c spl set id: b815792f-2f8f-7ac8-e053-2995a90ade18

Reported adverse events (FAERS/openFDA)#

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