PSP Witch hazel 85

Manufacturer: RW Consumer Products Ltd
Effective date: 2021-09-10
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 22:34:32

Label at a glance#

ProductPSP Witch hazel 85

Active ingredientWITCH HAZEL

Label structure7 sections

Indications and uses

Relieves minor skin irritations due to • insect bites • minor scrapes

Dosage and administration

• apply as often as needed

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Witch hazel 85%

Purpose

OTC - PURPOSE SECTION

Astringent

Uses

INDICATIONS & USAGE SECTION

Relieves minor skin irritations due to • insect bites • minor scrapes

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

• in the eyes. If contact occurs, rinse thoroughly with water.
• longer than one week unless directed by a doctor

Stop use and ask a doctor

OTC - STOP USE SECTION

if the condition persists or gets worse

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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

• apply as often as needed

Other information

SPL UNCLASSIFIED SECTION

do not use if induction seal under cap is broken or missing.

Inactive ingredients

INACTIVE INGREDIENT SECTION

ethyl alcohol, water

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label12

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

PSP Witch hazel 85
WITCH HAZEL
ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
69612-021	69612-021-01

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
ALCOHOL	3K9958V90M	IACT
WATER	059QF0KO0R	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
e0e1b078-7a83-497a-e053-2995a90a28f2			cba73cbf-5c46-729c-e053-2a95a90a5161	2022-06-07	Warnings	Exact identifier spl set id: cba73cbf-5c46-729c-e053-2a95a90a5161

Reported adverse events (FAERS/openFDA)#

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