AFIA FOAMING E2 SANITIZING HAND CLEANER- benzalkonium chloride soap 
National Chemical Laboratories, 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.

----------

Listing of Afia Foaming E2 Sanitizing Hand Cleaner

Drug Facts

Active Ingredient. Purpose

Benzalkonium Chloride 0.15%...........Antimicrobial hand Cleaner

Active

Uses

Uses

Warnings:

Warnings For external use only.

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water. Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Warnings

Directions

• Wet hands and wrist with water. Pump 2 strokes of foam into palm of hand. • Rub thoroughly over all surfaces of both hands and wrist, include between fingers and under cuticles, for 60 seconds. • Rinse hands completely and dry thoroughly.

Dosage

Inactive ingredients

Water / Cetrimonium Chloride / Coco Glucoside / Dihydroxyethyl Cocamine Oxide / Laurtrimonium Chloride / Glycereth-17 Cocoate / Cocamidopropyl Hydroxysultaine / Hydroxyethylcellulose / Citric Acid

Inactive ingredients

Uses

For hand-washing to decrease bacteria on the skin. Helps prevent cross contamination by hand contact.

uses

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Keep out of reach

Afia Foaming E2 Sanitizing Hand Cleaner

Final PackageCarton

AFIA FOAMING E2 SANITIZING HAND CLEANER 
benzalkonium chloride soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71023-448
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)  
HYDROXYETHYL CELLULOSE (5000 MPA.S AT 1%) (UNII: X70SE62ZAR)  
GLYCERETH-17 COCOATE (UNII: 3057VPT0KC)  
WATER (UNII: 059QF0KO0R)  
COCO GLUCOSIDE (UNII: ICS790225B)  
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71023-448-571000 mL in 1 BAG; Type 0: Not a Combination Product01/18/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/18/2017
Labeler - National Chemical Laboratories, Inc. (002289619)
Registrant - National Chemical Laboratories, Inc. (002289619)
Establishment
NameAddressID/FEIBusiness Operations
National Chemical Laboratories, Inc.002289619manufacture(71023-448)

Revised: 1/2017
Document Id: 466478c7-ea22-0f6c-e054-00144ff88e88
Set id: 466478c7-ea1d-0f6c-e054-00144ff88e88
Version: 2
Effective Time: 20170118
 
National Chemical Laboratories, Inc.