CVS Witch Hazel Spray

Manufacturer: CVS Pharmacy
Effective date: 2026-04-06
Label type: HUMAN OTC DRUG LABEL
Version: 8
Source: full-release
Hydrated at: 2026-06-01 01:52:48

Label at a glance#

ProductWitch Hazel

Active ingredientWITCH HAZEL

Label structure9 sections

Indications and uses

Relieves minor skin irritations due to: insect bites minor cuts minor scrapes

Dosage and administration

apply as often as needed to apply to face, moisten cotton ball or cleansing pad and gently wipe skin

Contacts and useful links#

PhoneLabel contact1-866-964-0939

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Witch Hazel 86%

Purpose

OTC - PURPOSE SECTION

Astringent

Uses

INDICATIONS & USAGE SECTION

Relieves minor skin irritations due to:

insect bites
minor cuts
minor scrapes

Warnings

WARNINGS SECTION

For external use only.

Flammable:

SAFE HANDLING WARNING SECTION

Keep away from heat, sparks, and open flame. Contents under pressure. Do not puncture or incinerate. Do not store at a temperature above 120°F.

When using this product

OTC - WHEN USING SECTION

avoid spraying in the eyes. If contact occurs rinse thoroughly with water
use only as directed
intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal.

Stop use and ask doctor of

OTC - ASK DOCTOR SECTION

condition worsens
symptoms last 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
to apply to face, moisten cotton ball or cleansing pad and gently wipe skin

Other Information

OTHER SAFETY INFORMATION

Store at room temperature

Inactive Ingredients

INACTIVE INGREDIENT SECTION

alcohol (14%)

Questions?

OTC - QUESTIONS SECTION

1-866-964-0939

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CVS

WITCH HAZEL

SPRAY

Astringent for Face & Body

Compare to

T.N. Dickinson's
Witch Hazel
active ingredient*

Relief of Minor
Skin Irritations Due to:
Insect bites, Minor cuts
& scrapes

NET WT 6 OZ (170 g)

carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1987674	witch hazel 86 % Topical Spray	PSN	8
1987674	witch hazel 860 MG/ML Topical Spray	SCD	8
1987674	witch hazel 86 % Topical Spray	SY	8

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
59779-765-17	Witch Hazel	170 g in 1 CAN	SPRAY	170		8

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
59779-765-17	GM - Gram	59779-765	87456eb0-34fe-4c9f-a63d-4a372316d986	1	2020-03-10

Products#

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

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

Witch Hazel
Witch Hazel Spray
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
59779-765	59779-765-17

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 SPRAY	CVS Pharmacy	53db78a8-eb2d-431b-84c1-73e99bb9d3d1	2026-04-06	Warnings	Exact identifier ndc (package): 59779-765-17 ndc (product): 59779-765 ndc11 (package): 59779076517 spl id: 4ecd909c-163a-6d56-e063-6294a90ad168 spl set id: 53db78a8-eb2d-431b-84c1-73e99bb9d3d1

Reported adverse events (FAERS/openFDA)#

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