ANTISEPTIC- benzalkonium chloride liquid 
Acme United Corporation

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.

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Drug Facts

Active Ingredients

Benzalkonium Chloride 0.13%

Purpose

Antiseptic

Uses

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

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 - Packet Label

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

Principal Display Panel - Box Label

J308
ANTISEPTICS

First Aid Only®

BZK Antiseptic
Towlettes

100 Wipes

Toallitas húmedas antisépticas
con cloruro de benzalconio

100 toallitas

Principal Display Panel - Box Label
ANTISEPTIC 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0924-7110
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
benzalkonium chloride (UNII: F5UM2KM3W7) (benzalkonium - UNII:7N6JUD5X6Y) benzalkonium chloride1.2478 g  in 1 L
Inactive Ingredients
Ingredient NameStrength
alcohol (UNII: 3K9958V90M)  
water (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0924-7110-0150 in 1 BOX
1NDC:0924-7110-000.0025 L in 1 PACKET; Type 0: Not a Combination Product
2NDC:0924-7110-0210 in 1 BOX
2NDC:0924-7110-000.0025 L in 1 PACKET; Type 0: Not a Combination Product
3NDC:0924-7110-0325 in 1 BOX
3NDC:0924-7110-000.0025 L in 1 PACKET; Type 0: Not a Combination Product
4NDC:0924-7110-0410 in 1 BOX
4NDC:0924-7110-000.0025 L in 1 PACKET; Type 0: Not a Combination Product
5NDC:0924-7110-0525 in 1 BOX
5NDC:0924-7110-000.0025 L in 1 PACKET; Type 0: Not a Combination Product
6NDC:0924-7110-0650 in 1 BOX
6NDC:0924-7110-000.0025 L in 1 PACKET; Type 0: Not a Combination Product
7NDC:0924-7110-07100 in 1 BOX
7NDC:0924-7110-000.0025 L in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E03/20/2012
Labeler - Acme United Corporation (001180207)
Registrant - Safetec of America, Inc. (874965262)
Establishment
NameAddressID/FEIBusiness Operations
Safetec of America, Inc.874965262MANUFACTURE(0924-7110)

Revised: 11/2015
Document Id: 38524256-4667-42db-85b9-d88cbc359dbe
Set id: 2a0fd7f2-73dd-499f-989e-24e6fb8a59bb
Version: 5
Effective Time: 20151120
 
Acme United Corporation