FDA.reportPublic FDA data

GOJO E2 Foam Sanitizing So ap

Manufacturer
GOJO Industries, Inc.
Effective date
2012-01-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:41:09

Label at a glance#

ProductGOJO E2 Foam Sanitizing So ap
Active ingredientTRICLOSAN
Label structure7 sections

Dosage and administration

Wet hands Apply a small amount of soap and work into a rich lather Rinse thoroughly with potable water Dry hands completely

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Triclosan 0.3%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Antiseptic cleanser to help reduce bacteria on skin that could cause disease

Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands
  • Apply a small amount of soap and work into a rich lather
  • Rinse thoroughly with potable water
  • Dry hands completely

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Alcohol, Lauric Acid, Propylene Glycol, Ethanolamine, Disodium Cocoamphodiacetate, Isopropyl Alcohol, Polyquaternium-10, Sodium Metabisulfite, Sodium Sulfite, Tetrasodium EDTA, Sodium Sulfate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product LabelProduct Label

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
21749-54321749-543-89, 21749-543-90, 21749-543-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
TRICLOSAN4NM5039Y5XACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT
LAURIC ACID1160N9NU9UIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
MONOETHANOLAMINE5KV86114PTIACT
DISODIUM COCOAMPHODIACETATE18L9G3U51MIACT
ISOPROPYL ALCOHOLND2M416302IACT
POLYQUATERNIUM-10 (1000 MPA.S AT 2%)GMR4PEN8PKIACT
SODIUM METABISULFITE4VON5FNS3CIACT
SODIUM SULFITEVTK01UQK3GIACT
EDETATE SODIUMMP1J8420LUIACT
SODIUM SULFATE0YPR65R21JIACT

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
6b64b777-1377-4e5f-903c-00970a2be5fd11483a33-1bb9-4c7f-8d16-b84064d4eec32024-03-21WarningsExact identifier
spl set id: 11483a33-1bb9-4c7f-8d16-b84064d4eec3

Reported adverse events (FAERS/openFDA)#

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