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Antiseptic by Acme United Corporation

Medically reviewed on November 20, 2017

Dosage form: liquid
Ingredients: benzalkonium chloride 1.2478g in 1L
Labeler: Acme United Corporation
NDC Code: 0924-7110

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.

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

ANTISEPTIC 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0924-7110
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
benzalkonium chloride (benzalkonium) benzalkonium chloride1.2478 g  in 1 L
Inactive Ingredients
Ingredient NameStrength
alcohol 
water 
Packaging
#Item CodePackage Description
1NDC:0924-7110-0150 PACKET in 1 BOX
1NDC:0924-7110-000.0025 L in 1 PACKET
2NDC:0924-7110-0210 PACKET in 1 BOX
2NDC:0924-7110-000.0025 L in 1 PACKET
3NDC:0924-7110-0325 PACKET in 1 BOX
3NDC:0924-7110-000.0025 L in 1 PACKET
4NDC:0924-7110-0410 PACKET in 1 BOX
4NDC:0924-7110-000.0025 L in 1 PACKET
5NDC:0924-7110-0525 PACKET in 1 BOX
5NDC:0924-7110-000.0025 L in 1 PACKET
6NDC:0924-7110-0650 PACKET in 1 BOX
6NDC:0924-7110-000.0025 L in 1 PACKET
7NDC:0924-7110-07100 PACKET in 1 BOX
7NDC:0924-7110-000.0025 L in 1 PACKET
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/FEIOperations
Safetec of America, Inc.874965262MANUFACTURE(0924-7110)

 
Acme United Corporation

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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