TRICLOSAN- 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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Active ingredient

Triclosan 0.3%

Purpose

Antimicrobial

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

Inactive ingredients

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

Product Label

TRICLOSAN 
triclosan liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-415
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)  
COCONUT ACID (UNII: 40U37V505D)  
SODIUM SULFATE (UNII: 0YPR65R21J)  
OLEIC ACID (UNII: 2UMI9U37CP)  
MONOETHANOLAMINE (UNII: 5KV86114PT)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
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)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:21749-415-101000 mL in 1 BAG; Type 0: Not a Combination Product03/10/2010
2NDC:21749-415-202000 mL in 1 BOX; Type 0: Not a Combination Product03/10/2010
3NDC:21749-415-16473 mL in 1 PACKAGE; Type 0: Not a Combination Product03/10/2010
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E03/10/201012/01/2021
Labeler - GOJO Industries, Inc. (004162038)
Registrant - GOJO Industries, Inc. (004162038)
Establishment
NameAddressID/FEIBusiness Operations
GOJO Industries, Inc.036424534manufacture(21749-415)

Revised: 10/2016
Document Id: d494364a-723f-48fc-b6c5-d8395444935c
Set id: 754b9722-3bb6-4f6f-9253-814a54b701aa
Version: 4
Effective Time: 20161014
 
GOJO Industries, Inc.