GOJO E2 FOAM SANITIZING SO AP- triclosan liquid 
GOJO Industries, Inc.

----------

GOJO E2 Foam Sanitizing Soap

Active ingredient

Triclosan 0.3%

Purpose

Antimicrobial

Use

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

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 soap and work into a rich lather
  • Rinse thoroughly with potable water
  • Dry hands completely

Inactive ingredients

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

Product label

GOJO E2 FOAM SANITIZING SO AP 
triclosan liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-543
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN0.003 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
LAURIC ACID (UNII: 1160N9NU9U)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
MONOETHANOLAMINE (UNII: 5KV86114PT)  
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK)  
SODIUM METABISULFITE (UNII: 4VON5FNS3C)  
SODIUM SULFITE (UNII: VTK01UQK3G)  
EDETATE SODIUM (UNII: MP1J8420LU)  
SODIUM SULFATE (UNII: 0YPR65R21J)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:21749-543-891200 mL in 1 PACKAGE; Type 0: Not a Combination Product01/01/201206/30/2022
2NDC:21749-543-901250 mL in 1 PACKAGE; Type 0: Not a Combination Product01/01/201206/30/2022
3NDC:21749-543-202000 mL in 1 PACKAGE; Type 0: Not a Combination Product01/01/201206/30/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM505(a)(3)01/01/201206/30/2022
Labeler - GOJO Industries, Inc. (004162038)
Establishment
NameAddressID/FEIBusiness Operations
GOJO Industries, Inc.036424534manufacture(21749-543)
Establishment
NameAddressID/FEIBusiness Operations
GOJO Industries, Inc.088312414label(21749-543) , pack(21749-543)

Revised: 3/2024
 
GOJO Industries, Inc.