GOJO E2 SANITIZING LTN SP- triclosan liquid
GOJO Industries, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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GOJO E2 Sanitizing Lotion Soap

Active ingredient

Triclosan 0.3%

Purpose

Antimicrobial

Use

• Handwash to help decrease bacteria on the skin

• Recommended for repeated use

Warnings

For external use only

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

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

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

Directions

• Wet hands

• Apply a small amount of product and work into a lather

• Rinse well and dry hands completely

Inactive ingredients

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

Product Label

GOJO E2 SANITIZING LTN SP
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:21749-135
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X)	TRICLOSAN	0.003 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
Water (UNII: 059QF0KO0R)
Coconut Acid (UNII: 40U37V505D)
Sodium Sulfate (UNII: 0YPR65R21J)
Oleic Acid (UNII: 2UMI9U37CP)
MONOETHANOLAMINE (UNII: 5KV86114PT)
COCO MONOETHANOLAMIDE (UNII: C80684146D)
Coco-Betaine (UNII: 03DH2IZ3FY)
Propylene Glycol (UNII: 6DC9Q167V3)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
EDETATE SODIUM (UNII: MP1J8420LU)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CORN OIL (UNII: 8470G57WFM)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
Methylchloroisothiazolinone (UNII: DEL7T5QRPN)
Methylisothiazolinone (UNII: 229D0E1QFA)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:21749-135-08	236 mL in 1 PACKAGE; Type 0: Not a Combination Product	09/17/2004	05/30/2022
2	NDC:21749-135-80	800 mL in 1 PACKAGE; Type 0: Not a Combination Product	09/17/2004	05/30/2022
3	NDC:21749-135-20	2000 mL in 1 PACKAGE; Type 0: Not a Combination Product	09/17/2004	05/30/2022
4	NDC:21749-135-37	3780 mL in 1 PACKAGE; Type 0: Not a Combination Product	09/17/2004	05/30/2022
5	NDC:21749-135-13	5000 mL in 1 PACKAGE; Type 0: Not a Combination Product	09/17/2004	05/30/2022
6	NDC:21749-135-54	208000 mL in 1 PACKAGE; Type 0: Not a Combination Product	09/17/2004	05/30/2022

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	09/17/2004	05/30/2022

Labeler - GOJO Industries, Inc. (004162038)

Name	Address	ID/FEI	Business Operations
Establishment
GOJO Industries, Inc.		036424534	manufacture(21749-135)

Name	Address	ID/FEI	Business Operations
Establishment
GOJO Industries, Inc.		088312414	label(21749-135) , pack(21749-135)

Revised: 8/2020

Document Id: c9f6b5d4-0a37-4a9b-bfae-1cc13ef5cfc7

Set id: 12e267be-b982-47c4-83ff-600021f3fec1

Version: 2

Effective Time: 20200827

GOJO Industries, Inc.