ZEP MANGO FOAMING- triclosan liquid 
Zep 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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Zep Professional Foaming Antibacterial Hand Soap

Active ingredient

Triclosan 0.1%

Purpose

Antiseptic Handwash

Uses

For handwashing to decrease bacteria on this skin.

Warnings

For external use only.

Do not use in the eyes.

When using this product

  • if swallowed, seek medical attention.
  • if eye contact occurs, flush eyes with water and consult a physician.

Discontinue use if irritation and redness develop.

If condition persists for more than 72 hours, consult a doctor.

Keep out of reach of children.

Directions

  • press pump to dispense product onto hands, lather and rinse.

Other information

  • Store at room temperature
  • Do not freeze

Inactive ingredients

Water, Ammonium Lauryl Sulfate, Ammonium Laureth-3 Sulfate, Cocamide DIPA, Disodium Ricinoleic MEA Sulfosuccinate, Fragrance, Glycerin, Tetrasodium EDTA, Methylchloroisothiazolinone (and) Methylisothiazolinone, Citric Acid, Glutaral, Yellow 5, Red 4

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ZEP MANGO FOAMING 
triclosan liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-277
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN0.01 g  in 10 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)  
AMMONIUM LAURETH-3 SULFATE (UNII: 896SJ235FN)  
COCO DIISOPROPANOLAMIDE (UNII: S485AM948Q)  
DISODIUM RICINOLEIC MONOETHANOLAMIDE SULFOSUCCINATE (UNII: 1YHW4GJC3U)  
GLYCERIN (UNII: PDC6A3C0OX)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
GLUTARAL (UNII: T3C89M417N)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66949-277-01550 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/01/201001/02/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A02/01/201001/02/2019
Labeler - Zep Inc. (030471374)
Establishment
NameAddressID/FEIBusiness Operations
Zep Inc.030471374manufacture(66949-277)

Revised: 11/2016
Document Id: 40b92e12-8e1b-4fd7-e054-00144ff88e88
Set id: 7549b92d-67a0-4f91-955c-42242ccdff11
Version: 3
Effective Time: 20161107
 
Zep Inc.