FDA.reportPublic FDA data

PSP GO

Manufacturer
RW Consumer Products Ltd
Effective date
2021-09-10
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:36:40

Label at a glance#

ProductPSP GO
Active ingredientWITCH HAZEL
Label structure7 sections

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

Use

INDICATIONS & USAGE SECTION

relieves minor skin irritations due to: • insect bites • minor scrapes

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

  • Avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

  • Conditions 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

Other Information

SPL UNCLASSIFIED SECTION

  • Do not use if shrink band around cap is broken or missing

Inactive Ingredients

INACTIVE INGREDIENT SECTION

ethyl alcohol, water

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69612-00669612-006-03

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
NameUNIIKind
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
WITCH HAZEL101I4J0U34ACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
e06a3f72-a397-0118-e053-2a95a90a6cb25367376c-70bc-45c7-afed-413645fc18322022-06-01WarningsExact identifier
spl set id: 5367376c-70bc-45c7-afed-413645fc1832

Reported adverse events (FAERS/openFDA)#

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