FDA.reportPublic FDA data

Go PSP hand sanitizer

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 22:34:31

Label at a glance#

ProductGo PSP hand sanitizer
Active ingredientISOPROPYL ALCOHOL
Label structure7 sections

Dosage and administration

Spray directly on hands and rub in thoroughly over 30 seconds Allow to dry For children under 6, use adult supervision  Not recommended for infants

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

  • Helps reduce bacteria on the skin
  • Recommended for repeated use

Warnings

WARNINGS SECTION

Flammable, keep away from fire or flame.
For external use only.

When using this product

OTC - WHEN USING SECTION

  • Keep out of eyes 
  • In case of contact with eyes, flush thoroughly with water
  • Avoid contact with broken skin 
  • Do not inhale or ingest

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • Irritation and redness develop and persist for more than 72 hours

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

  • Spray directly on hands and rub in thoroughly over 30 seconds
  • Allow to dry
  • For children under 6, use adult supervision 
  • Not recommended for infants

Other Information

SPL UNCLASSIFIED SECTION

  • Do not store above 104°F/40°C
  • Do not use if shrink band around cap is broken or missing

Inactive ingredients

INACTIVE INGREDIENT SECTION

glycerin, hydrogen peroxide, purified 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 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69612-01169612-011-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
HYDROGEN PEROXIDEBBX060AN9VIACT
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302ACTIB

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
df736abd-9cee-4e90-e053-2995a90aab5ecba66231-f8a0-2d03-e053-2a95a90a29ce2022-05-20WarningsExact identifier
spl set id: cba66231-f8a0-2d03-e053-2a95a90a29ce

Reported adverse events (FAERS/openFDA)#

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