WITCH HAZEL

Manufacturer: CHAIN DRUG MARKETING ASSOCIATION INC | Seaway Pharma Inc.
Effective date: 2024-12-26
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 00:49:17

Label at a glance#

ProductWITCH HAZEL

Active ingredientWITCH HAZEL

Label structure10 sections

Dosage and administration

apply as often as needed

Contacts and useful links#

PhoneLabel contact1-800-935-2362

Websitewww.qualitychoice.com

www.qualitychoice.com

Label contents#

Full prescribing information#

Active Ingredient Purpose

OTC - ACTIVE INGREDIENT SECTION

Witch hazel ................................................Astringent

OTC - PURPOSE SECTION

Gentle Relief for:
Oily, Irritated, Red, Damaged, Blemished, or Inflamed Skin

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

avoid contact with eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition worsens or symptoms persist for more than 7 days

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help, or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

apply as often as needed

Inactive ingredients

INACTIVE INGREDIENT SECTION

alcohol and purified water

SPL UNCLASSIFIED SECTION

Questions or comments?
1-800-935-2362 (Mon-Fri 9am-5pm EST)

Distributed by C.D.M.A. lnc.
43157 W 9 Mile Rd
Novi, MI 48375
www.qualitychoice.com

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63868-592-16	WITCH HAZEL	473 mL in 1 BOTTLE	SOLUTION	473		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63868-592	WITCH HAZEL SOLUTION [CHAIN DRUG MARKETING ASSOCIATION INC]	2	Current NDC, Legacy NDC, 1 package rows	20241228_bdccee3f-0ad8-4264-a65f-ae86aed6bf03.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
63868-592-16	ML - Milliliter	63868-592	e46f4f99-6bc0-4a64-82d0-363aa0d40992	1	2022-10-06

Products#

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

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

WITCH HAZEL
WATER
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
63868-592	63868-592-16

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
WITCH HAZEL	101I4J0U34	ACTIB
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	IACT

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	CHAIN DRUG MARKETING ASSOCIATION INC	bdccee3f-0ad8-4264-a65f-ae86aed6bf03	2024-12-26	Warnings	Exact identifier ndc (package): 63868-592-16 ndc (product): 63868-592 ndc11 (package): 63868059216 spl id: 367a5404-a427-4b41-8776-ce54bbb370ab spl set id: bdccee3f-0ad8-4264-a65f-ae86aed6bf03

Reported adverse events (FAERS/openFDA)#

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