ZEP FS ANTIMICROBIAL FOAMING HAND CLEANER- benzalkonium chloride 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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66949-996 FS Antimicrobial Foaming

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antiseptic Hand Wash

Uses

  • Hand washing to decrease bacteria on the skin.
  • For use in food processing facilities.

Warnings

For external use only.

Do not use in the eyes; if in eyes, rinse promptly and thoroughly with water.

Stop use and ask doctor if skin irritation or redness persists for more than 72 hours.

  • Do not swallow.
  • If swallowed, do not induce vomiting and if individual is conscious, give large quantities of water to drink and consult a physician immediately.

Keep out of reach of children and pets. Children must be supervised in use of this product.

Directions

  • Wet hands with water.
  • Place hands under dispenser and apply liquid soap.
  • Massage soap into hands and writsts, emphasizing back of hands, knuckles and cuticles.
  • Rise hands thoroughly and dry.

Other information

  • Store at 20 to 25°C (68 to 77°F).
  • Do not freeze.
  • Dispose in accordance with all applicable federal, state and local regulations.

Inactive ingredients

Water, Cocamidopropyl Hydroxysultaine, Lauramine Oxide, Didecyldimonium Chloride, PEG-6 Cocamide, Phenoxyethanol, Iodopropynyl Butylcarbamate, Methylisothiazolinone, Hexanediol

Questions or comments?

Call 1-800-I-BUY-ZEP (1-800-428-9937)

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ZEP FS ANTIMICROBIAL FOAMING HAND CLEANER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-996
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
HEXANEDIOL (UNII: ZIA319275I)  
WATER (UNII: 059QF0KO0R)  
COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)  
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
PEG-6 COCAMIDE (UNII: YZ6NLA4O1E)  
DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66949-996-116000 mL in 1 CASE; Type 0: Not a Combination Product04/12/200612/31/2020
2NDC:66949-996-1610000 mL in 1 CASE; Type 0: Not a Combination Product04/12/200612/31/2020
3NDC:66949-996-85208198 mL in 1 DRUM; Type 0: Not a Combination Product04/12/200612/31/2020
4NDC:66949-996-171200 mL in 1 CASE; Type 0: Not a Combination Product04/12/200612/31/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A04/12/200612/31/2020
Labeler - Zep Inc. (030471374)
Establishment
NameAddressID/FEIBusiness Operations
Zep Inc.112125310manufacture(66949-996)

Revised: 11/2020
Document Id: b4644afc-498c-5e01-e053-2995a90a3485
Set id: 1bd42afd-4ac2-4a05-86cc-b65f399a85b2
Version: 11
Effective Time: 20201118
 
Zep Inc.