MED NAP BENZALKONIUM CHLORIDE 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.

----------

Med Nap Benzalkonium Chloride Antiseptic Towelette

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

First Aid Antiseptic

Uses

First Aid antiseptic to help prevent infection in minor

•cuts
•scrapes
•burns

Warnings



For External Use Only.

Do not use

•in the eyes
•over large areas of the body
•longer than 1 week

Ask a doctor before use if you have •Deep or puncture wounds •Animal bites •Serious burns

Stop use

Stop use and ask doctor if the condition persists or gets worse.

.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control center right away.

Directions

To open: Tear packet open at notch, remove towelette, use it only once

•Clean affected area
•Apply 1 to 3 times daily
•May be covered with a sterile bandage, once area dries

Other Information

Store at room temperature

Inactive Ingredients

methylchloroisothiazolinone/methylisothiazolinone mixture, water

1.800.835.2263

Box Label Box Label

MED NAP BENZALKONIUM CHLORIDE ANTISEPTIC 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0924-0246
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.0018 mg  in 1.35 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0924-0246-001.35 mL in 1 PACKET; Type 0: Not a Combination Product02/11/2022
2NDC:0924-0246-01100 in 1 BOX02/11/2022
21.35 mL in 1 PACKET; Type 0: Not a Combination Product
3NDC:0924-0246-021000 in 1 BOX02/11/2022
31.35 mL in 1 PACKET; Type 0: Not a Combination Product
4NDC:0924-0246-0312000 in 1 BOX02/11/2022
41.35 mL in 1 PACKET; Type 0: Not a Combination Product
5NDC:0924-0246-0420 in 1 BOX02/28/2023
51.35 mL in 1 PACKET; Type 0: Not a Combination Product
6NDC:0924-0246-0525 in 1 BOX02/28/2023
61.35 mL in 1 PACKET; Type 0: Not a Combination Product
7NDC:0924-0246-0660000 in 1 CONTAINER02/28/2023
71.35 mL in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E02/11/2022
Labeler - Acme United Corporation (001180207)
Establishment
NameAddressID/FEIBusiness Operations
Acme United Corporation117825595manufacture(0924-0246)

Revised: 2/2023
Document Id: f54f5472-4e35-80b8-e053-2995a90aee0c
Set id: d7c404c1-c765-a67c-e053-2995a90a6b8e
Version: 2
Effective Time: 20230222
 
Acme United Corporation