ZEP ACCLAIM- 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 Acclaim

Active ingredient

Triclosan 0.1%

Purpose

Antiseptic Handwash

Uses

Hand washing to decrease bacteria on skin.

Warnings

For external use only.

Do not use in or around eyes.

When using this product

  • If eye contact occurs, rinse promptly and thoroughly with water.
  • If swallowed, seek medical attention.

Discontinue use if irritation and redness develops. If condition persists for more than 72 hours, consult a doctor.

Keep out of reach of children.

Directions

  • Wet hands with water
  • Place hands under dispenser
  • Apply liquid soap
  • Massage soap into hands and wrists, emphasizing back of hands, knuckles and cuticles
  • Rinse thoroughly

Other information

  • Store at room temperature
  • Do not freeze

Inactive ingredients

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

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ZEP ACCLAIM 
triclosan liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-999
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)  
AMMONIUM CHLORIDE (UNII: 01Q9PC255D)  
DISODIUM RICINOLEIC MONOETHANOLAMIDE SULFOSUCCINATE (UNII: 1YHW4GJC3U)  
GLYCERIN (UNII: PDC6A3C0OX)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
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:66949-999-00500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/29/199501/01/2019
2NDC:66949-999-101000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/29/199501/01/2019
3NDC:66949-999-213785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/29/199501/01/2019
4NDC:66949-999-15946.353 mL in 1 BOTTLE; Type 0: Not a Combination Product03/29/199501/01/2019
5NDC:66949-999-891040990 mL in 1 CONTAINER; Type 0: Not a Combination Product03/29/199501/01/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/29/199501/01/2019
Labeler - Zep Inc. (030471374)
Establishment
NameAddressID/FEIBusiness Operations
Zep Inc.030471374manufacture(66949-999)

Revised: 11/2016
Document Id: 40f7fe23-6817-43d7-e054-00144ff8d46c
Set id: a3e8ef7c-c0f5-4708-8cb0-758e496b70b0
Version: 5
Effective Time: 20161110
 
Zep Inc.