HAND ANTIBACTERIAL WIPES- benzalkonium chloride cloth

Hand Antibacterial Wipes by

Drug Labeling and Warnings

Hand Antibacterial Wipes by is a Otc medication manufactured, distributed, or labeled by Namco Manufacturing INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient(s)

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial Agent

Use

Decreases bacteria on skin.

Warnings

For external use only.

Do not use

Do not use if you are allergic to any of the ingredients.

WHEN USING

Using this product do not get into eyes. lf contact occurs, rinse thoroughly with water.

STOP USE

Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.

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.

Directions

Tear open dispensing cap and remove entire lid from canister.

Locate wipe at center of the roll,twist corner to a point and thread through small opening in lid.

Replace lid and pull wipe up at an angle.Remaining wipes feed automatically.

Snap lid cap shut to retain moisture when finished.

Inactive ingredients

C12-14 Alkyl Dimethyl, Ethylbenzyl Ammonium Chloride, Alkyl Polyglucoside, Disodium EDTA, Propylene Glycol, Aqua.

Package Label - Principal Display Panel

NDC: 79530-003-01

NDC: 79530-003-02

INGREDIENTS AND APPEARANCE

HAND ANTIBACTERIAL WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79530-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM CHLORIDE (C12-C14) (UNII: G258TFN61X)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
EDETATE DISODIUM (UNII: 7FLD91C86K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79530-003-01	3360 g in 1 PAIL; Type 0: Not a Combination Product	07/11/2020
2	NDC: 79530-003-02	270 g in 1 PAIL; Type 0: Not a Combination Product	08/27/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	07/11/2020

Labeler - Namco Manufacturing INC. (058595448)