AFIA FOAMING E2 SANITIZING HAND CLEANER- benzalkonium chloride soap

Afia Foaming E2 Sanitizing Hand Cleaner by

Drug Labeling and Warnings

Afia Foaming E2 Sanitizing Hand Cleaner by is a Otc medication manufactured, distributed, or labeled by National Chemical Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient. Purpose

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

Uses

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

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.

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.

Inactive ingredients

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

Uses

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

KEEP OUT OF REACH OF CHILDREN

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

PRINCIPAL DISPLAY PANEL

Afia Foaming E2 Sanitizing Hand Cleaner

INGREDIENTS AND APPEARANCE

AFIA FOAMING E2 SANITIZING HAND CLEANER 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71023-448
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71023-448-57	1000 mL in 1 BAG; Type 0: Not a Combination Product	01/18/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/18/2017

Labeler - National Chemical Laboratories, Inc. (002289619)

Registrant - National Chemical Laboratories, Inc. (002289619)

Establishment
Name	Address	ID/FEI	Business Operations
National Chemical Laboratories, Inc.		002289619	manufacture(71023-448)