FDA.reportPublic FDA data

TRICLOSAN

Manufacturer
GOJO Industries, Inc.
Effective date
2016-10-14
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-02 00:20:14

Label at a glance#

ProductTRICLOSAN
Active ingredientTRICLOSAN
Label structure7 sections

Dosage and administration

Wet hands Apply a small amount of product and work into a lather Rinse well and 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

  • Handwash to help decrease bacteria on the skin
  • 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 product and work into a lather
  • Rinse well and dry hands completely

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Coconut Acid, Sodium Sulfate, Oleic Acid, Ethanolamine, Aloe Barbadensis Leaf Juice, Cocamide MEA, Coco-Betaine, Hydrolyzed Vegetable Protein, Propylene Glycol, Retinyl Palmitate, Tetrasodium EDTA, Tocopheryl Acetate, Zea Mays (Corn) Oil, Hydroxypropyl Methylcellulose, Methylchloroisothiazolinone, Methylisothiazolinone

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product LabelProduct Label

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
TRICLOSANACTIVE INGREDIENT4NM5039Y5X3
TRICLOSANACTIVE MOIETY4NM5039Y5X3

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
21749-41521749-415-10, 21749-415-20, 21749-415-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
TRICLOSAN4NM5039Y5XACTIB
WATER059QF0KO0RIACT
COCONUT ACID40U37V505DIACT
SODIUM SULFATE0YPR65R21JIACT
OLEIC ACID2UMI9U37CPIACT
MONOETHANOLAMINE5KV86114PTIACT
ALOE VERA LEAFZY81Z83H0XIACT
COCO MONOETHANOLAMIDEC80684146DIACT
COCO-BETAINE03DH2IZ3FYIACT
Propylene Glycol6DC9Q167V3IACT
VITAMIN A PALMITATE1D1K0N0VVCIACT
EDETATE SODIUMMP1J8420LUIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
CORN OIL8470G57WFMIACT
HYPROMELLOSE, UNSPECIFIED3NXW29V3WOIACT
MethylchloroisothiazolinoneDEL7T5QRPNIACT
Methylisothiazolinone229D0E1QFAIACT

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
d494364a-723f-48fc-b6c5-d8395444935c754b9722-3bb6-4f6f-9253-814a54b701aa2016-10-14WarningsExact identifier
spl id: d494364a-723f-48fc-b6c5-d8395444935c
spl set id: 754b9722-3bb6-4f6f-9253-814a54b701aa

Reported adverse events (FAERS/openFDA)#

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