Equaline 822.002/822AA

Manufacturer: United Natural Foods, Inc. dba UNFI | Nice-Pak Products, LLC
Effective date: 2026-08-28
Label type: HUMAN OTC DRUG LABEL
Version: 20
Source: daily-update
Hydrated at: 2026-09-01 13:02:58

Label at a glance#

ProductWitch Hazel

Active ingredientWITCH HAZEL

Label structure12 sections

Dosage and administration

apply as often as needed

Contacts and useful links#

PhoneLabel contact855-423-2630

Label contents#

Full prescribing information#

Claims

SPL UNCLASSIFIED SECTION

cleans and refreshens skin
tones skin
soothes sunburn

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Witch hazel 100%
(containing alcohol 14% by volume)

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 persist 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

None

Adverse event

ADVERSE REACTIONS SECTION

Like it or let us make it right.

That's our quality promise.

855-423-2630

DISTRIBUTED BY UNFI

PROVIDENCE, RI 02903 USA

Pat. D675, 101

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

EQUALINE ^®

witch hazel

astringent

hamamelis water

for relief of minor skin irritations due to:

insect bites
minor cuts
minor scrapes

16 FL OZ (1 PT) 473 mL

image descriptionimage description

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Data code	Data Matrix	L0003483FC		mm01.jpg

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
41163-822-43	ML - Milliliter	41163-822	96870c99-f003-4c72-85bb-d22d133ede7b	1	2016-12-07

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
WITCH HAZEL	ACTIVE INGREDIENT	101I4J0U34	3
WITCH HAZEL	ACTIVE MOIETY	101I4J0U34	3
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	3

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
41163-822	41163-822-43

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

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
19	2026-02-17	full-release	2026-06-01 01:46:15

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / TOPICAL		2445 mg	Exact identifier — unii+route+dosage form 2 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / TOPICAL		2445 mg	Exact identifier — unii+route+dosage form 2 equally ranked IID candidates

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	United Natural Foods, Inc. dba UNFI	d2d1bd9e-7025-4151-95f2-a2f521dc2be8	2026-08-28	Warnings, Adverse reactions	Exact identifier ndc (package): 41163-822-43 ndc (product): 41163-822 ndc11 (package): 41163082243 spl id: 5a1d8c66-d618-9cbe-e063-6394a90ab118 spl set id: d2d1bd9e-7025-4151-95f2-a2f521dc2be8

Reported adverse events (FAERS/openFDA)#

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