Med Nap Benzalkonium Chloride Antiseptic Towelette

MED NAP Benzalkonium Chloride Antiseptic by

Drug Labeling and Warnings

MED NAP Benzalkonium Chloride Antiseptic by is a Otc medication manufactured, distributed, or labeled by Acme United Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MED NAP BENZALKONIUM CHLORIDE ANTISEPTIC- benzalkonium chloride liquid 
Acme United Corporation

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Med Nap Benzalkonium Chloride Antiseptic Towelette

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antiseptic

Caution:

Keep out of reach of children.

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

Use:

First aid antisepticto help prevent skin infection in Minor Cuts Scrapes Burns

Antiseptic Cleansing Perineal and maternity care.

Warnings



For External Use Only.

Do not use As an antiseptic for more than 1 week in or around the eyes Over large areas of the body.

Stop use

if irritation and redness develop if condition persists more than 72 hours, consult a physician.

.

Directions

Tear at notch Remove towelette Use only once

As a first aid antiseptic Clean affected area Apply 1 to 3 times daily May be covered with a sterile bandage If bandaged, let dry first

Other Information

Store at room temperature Avoid excessive heat

Inactive Ingredients

Water, methylchloroisothiazolinone, methylisothiazolinone

Box Image

Box Image

MED NAP BENZALKONIUM CHLORIDE ANTISEPTIC 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 0924-0245
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1.7 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
MAGNESIUM CHLORIDE ANHYDROUS (UNII: 59XN63C8VM)  
MAGNESIUM NITRATE (UNII: 77CBG3UN78)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 0924-0245-001.7 mL in 1 PACKET; Type 0: Not a Combination Product07/09/2021
2NDC: 0924-0245-021000 in 1 BOX07/09/2021
2NDC: 0924-0245-001.7 mL in 1 PACKET; Type 0: Not a Combination Product
3NDC: 0924-0245-01100 in 1 BOX07/09/2021
3NDC: 0924-0245-001.7 mL in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00307/09/202106/07/2023
Labeler - Acme United Corporation (001180207)
Establishment
NameAddressID/FEIBusiness Operations
Acme United Corporation117825595manufacture(0924-0245)

Revised: 1/2025
Document Id: 2d0511f4-a9f8-b373-e063-6394a90a8878
Set id: c6b4850d-cbf0-048d-e053-2995a90ab22d
Version: 2
Effective Time: 20250131