ANTISEPTIC- benzalkonium chloride liquid

Antiseptic by

Drug Labeling and Warnings

Antiseptic by is a Otc medication manufactured, distributed, or labeled by Acme United Corporation, Safetec of America, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

Benzalkonium Chloride 0.13%

Purpose

Antiseptic

Uses

• Antiseptic cleansing of face, hands and body to decrease bacteria on skin without soap and water

Warnings

For external use only

Do not use in the eyes. If this happens, rinse thoroughly with water.

Stop use and ask doctor if irritation or redness develop and 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

• tear open packet, unfold and use as a washcloth. Allow hands to dry without wiping.

Inactive ingredients

Purified water, alcohol

Principal Display Panel - Packet Label

FIRST AID ONLY®

Antiseptic
Towelette

Benzalkonium Chloride (BZK)

1 Premoistened Towelette

Package not Child-Resistant

www.FirstAidOnly.com

Fairfield, CT 06824

1.800.835.2263

© 2015 Acme United Corporation.

Principal Display Panel - Box Label

FIRST AID ONLY®

51028

ANTISEPTICS

BZK Antiseptic Towelettes

25 Wipes

Toallitas húmedas antisépticas con cloruro de benzalconio

25 toallitas

Principal Display Panel - Box Label

J308
ANTISEPTICS

First Aid Only®

BZK Antiseptic
Towlettes

100 Wipes

Toallitas húmedas antisépticas
con cloruro de benzalconio

100 toallitas

INGREDIENTS AND APPEARANCE

ANTISEPTIC 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0924-7110
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
benzalkonium chloride (UNII: F5UM2KM3W7) (benzalkonium - UNII:7N6JUD5X6Y)	benzalkonium chloride	1.2478 g  in 1 L

Inactive Ingredients
Ingredient Name	Strength
alcohol (UNII: 3K9958V90M)
water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0924-7110-01	50 in 1 BOX
1	NDC: 0924-7110-00	0.0025 L in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 0924-7110-02	10 in 1 BOX
2	NDC: 0924-7110-00	0.0025 L in 1 PACKET; Type 0: Not a Combination Product
3	NDC: 0924-7110-03	25 in 1 BOX
3	NDC: 0924-7110-00	0.0025 L in 1 PACKET; Type 0: Not a Combination Product
4	NDC: 0924-7110-04	10 in 1 BOX
4	NDC: 0924-7110-00	0.0025 L in 1 PACKET; Type 0: Not a Combination Product
5	NDC: 0924-7110-05	25 in 1 BOX
5	NDC: 0924-7110-00	0.0025 L in 1 PACKET; Type 0: Not a Combination Product
6	NDC: 0924-7110-06	50 in 1 BOX
6	NDC: 0924-7110-00	0.0025 L in 1 PACKET; Type 0: Not a Combination Product
7	NDC: 0924-7110-07	100 in 1 BOX
7	NDC: 0924-7110-00	0.0025 L in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/20/2012

Labeler - Acme United Corporation (001180207)

Registrant - Safetec of America, Inc. (874965262)

Establishment
Name	Address	ID/FEI	Business Operations
Safetec of America, Inc.		874965262	MANUFACTURE(0924-7110)