AFIA FOAMING ANTI-BACTERIAL HAND CLEANER- chloroxylenol soap

Afia Foaming Anti-Bacterial Hand Cleaner by

Drug Labeling and Warnings

Afia Foaming Anti-Bacterial 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

Chloroxylenol 0.3%............Antimicrobial

Uses

For hand washing to decrease bacteria on the skin

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.

Directions

• Wet a hand. Pump one or two stokes of foam, into palm of hand.
• Rub thoroughly over all surfacesof both hands for 30 seconds
• Rinse hands and dry thoroughly.

Inactive ingredients

Water, Sodium Methyl 2-Sulfolaurate, Disodium 2-Sulfolaurate, Decyl glucoside, Cocamidopropyl Betaine, Lauric Monoethanolamide, Cetrimonium Chloride, PEG-150 Distearate, Phenoxyethanol, fragrance, Methylchloroisothiazolinone, Methylisothiazolinone, FD&C yellow #5, FD&C blue #1

Warnings:

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

Uses

For hand washing to decrease bacteria on the skin

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AFIA FOAMING ANTI-BACTERIAL HAND CLEANER 
chloroxylenol soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71023-446
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
DISODIUM 2-SULFOLAURATE (UNII: 329M3829G2)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
WATER (UNII: 059QF0KO0R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM METHYL 2-SULFOLAURATE (UNII: I39GGJ23HV)
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
LAURIC MONOETHANOLAMIDE (UNII: 098P2IGT76)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71023-446-57	1000 mL in 1 BAG; Type 0: Not a Combination Product	10/24/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	10/24/2016

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(71023-446)