BENZALKONIUM CHLORIDE swab

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)

Available from:

Professional Disposables International, Inc.

INN (International Name):

BENZALKONIUM CHLORIDE

Composition:

BENZALKONIUM CHLORIDE 0.0013 g in 1 mL

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

For hand washing to decrease bacteria on the skin. Antiseptic handwash

Authorization status:

OTC monograph not final

Summary of Product characteristics

BENZALKONIUM CHLORIDE- BENZALKONIUM CHLORIDE SWAB
PROFESSIONAL DISPOSABLES INTERNATIONAL, 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._
----------
HYGEA BENZALKONIUM CHLORIDE ANTISEPTIC TOWELETTE 10819-3740
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
Aloe Barbadensis Leaf Juice, Disodium EDTA, Potassium Sorbate, PPG-2
Hydroxyethyl
Cocamide, Purified Water
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
PACKET
BOX
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)
BENZ ALKONIUM
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 DESCRI