Premier Solutions Witch Hazel Spray

Manufacturer: Premier Brands of America Inc.
Effective date: 2025-11-03
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 01:41:52

Label at a glance#

ProductWitch Hazel

Active ingredientWITCH HAZEL

Label structure10 sections

Indications and uses

Relieves minor skin irritation 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 irritation 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 harful or fatal.

Stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

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

Other information

OTHER SAFETY INFORMATION

store at room temperature

Inactive ingredient

INACTIVE INGREDIENT SECTION

alcohol (14%)

Questions?

OTC - QUESTIONS SECTION

Call 1-866-964-0939

RECENT MAJOR CHANGES SECTION

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

premier

solutions

WITCH

HAZEL

CONTINUOUS SPRAY

WITCH HAZEL 86%/

ASTRINGENT

NATURAL ASTRINGENT

FOR FACE & BODY

Cleanses & soothes

irritated,inflamed, oily,

or blemished skin

NET WT. 6.0 0Z. (170 g)

carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1987674	witch hazel 86 % Topical Spray	PSN	2
1987674	witch hazel 860 MG/ML Topical Spray	SCD	2
1987674	witch hazel 86 % Topical Spray	SY	2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
56104-904-01	Witch Hazel	170 g in 1 CAN	SPRAY	170		2

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
56104-904	56104-904-01

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
1	2025-06-23	full-release	2026-06-01 01:03:49

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	Premier Brands of America Inc.	38583c02-497b-922c-e063-6294a90a49de	2025-11-03	Warnings	Exact identifier ndc (package): 56104-904-01 ndc (product): 56104-904 ndc11 (package): 56104090401 spl id: 42b885ee-203a-2e7a-e063-6394a90ad29b spl set id: 38583c02-497b-922c-e063-6294a90a49de

Reported adverse events (FAERS/openFDA)#

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