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 Type HUMAN OTC DRUG Item Code (Source) NDC:21749-415
Route of Administration TOPICAL
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN 0.003 mg  in 1 mL
Inactive Ingredients
Ingredient Name Strength
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 Code Package Description Marketing Start Date Marketing End Date
1 NDC:21749-415-10 1000 mL in 1 BAG; Type 0: Not a Combination Product 03/10/2010
2 NDC:21749-415-20 2000 mL in 1 BOX; Type 0: Not a Combination Product 03/10/2010
3 NDC:21749-415-16 473 mL in 1 PACKAGE; Type 0: Not a Combination Product 03/10/2010
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 03/10/2010 12/01/2021
Labeler - GOJO Industries, Inc. (004162038)
Registrant - GOJO Industries, Inc. (004162038)
Establishment
Name Address ID/FEI Business Operations
GOJO Industries, Inc. 036424534 manufacture(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.