BENZALKONIUM CHLORIDE swab

Benzalkonium Chloride by

Drug Labeling and Warnings

Benzalkonium Chloride by is a Otc medication manufactured, distributed, or labeled by Professional Disposables International, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

USE

For hand washing to decrease bacteria on the skin.

PURPOSE

Antiseptic handwash

WARNINGS

• For external use only.
• If swallowed, get medical help or contact a Poison Control Center right away.
• Discontinue use if irritation and redness develop. If condition persists for more than 72 hours consult a doctor.
• Do not use in the eyes.

Keep out of reach of children.

Keep out of reach of children.

DIRECTIONS

• Tear open packet.
• Unfold and use; discard in trash receptacle after single use.
• Wet hands thoroughly with product and allow to dry without wiping.

OTHER INFORMATION

Lot number and expiration date can be found on back panel of packet.

INACTIVE INGREDIENTS

Purified Water, Potassium Sorbate, PPG-2 Hydroxyethyl Cocamide, Disodium EDTA, Aloe Barbadensis Leaf Juice

SPL UNCLASSIFIED SECTION

Professional Disposables International, Inc.
Orangeburg, NY 10962-1376 - USA - 1-800-999-6423
Made in USA

ACTIVE INGREDIENT

Benzalkonium Chloride, 0.13% w/w

DOSAGE

Wet hands thoroughly with product and allow to dry without wiping.

PRINCIPAL DISPLAY PANEL-100 COUNT

Hygea
Benzalkonium Chloride
Antiseptic Towelette

1 Towelette [7.0 x 5.0 in (17.7 x 12.7 cm)] 100 Towelettes per Box

Packet Label

Box Label

INGREDIENTS AND APPEARANCE

BENZALKONIUM CHLORIDE 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10819-3740
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.0013 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
COCO DIETHANOLAMIDE (UNII: 92005F972D)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10819-3740-1	3 mL in 1 PACKET; Type 1: Convenience Kit of Co-Package	01/01/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/01/2012

Labeler - Professional Disposables International, Inc. (800777117)

Establishment
Name	Address	ID/FEI	Business Operations
Professional Disposables International, Inc.		800777117	manufacture(10819-3740)