MED NAP CLEANSING TOWELETTE- benzalkonium chloride liquid

MED NAP Cleansing Towelette by

Drug Labeling and Warnings

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

Drug Details [pdf]

Drug Facts Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

First Aid antiseptic

Use:

First Aid antiseptic to help prevent infection in minor

cuts
scrapes
burns

Caution:

Keep out of reach of children.

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

Warnings

For external use only

Do not use ▪in the eyes ▪over large areas of the body longer than 1 week

Stop use

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

ASK DOCTOR

Ask doctor before use if you have

deep or puncture wounds
animal bites
serious burns

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

isopropyl alcohol, methylchloroisothiazolinone/methylisothiazolinone mixture, water

QUESTIONS

Questions? 1.800.835.2263

PRINCIPAL DISPLAY PANEL

Box Image

INGREDIENTS AND APPEARANCE

MED NAP CLEANSING TOWELETTE 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0924-0243
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.0018 mg  in 1.35 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
ISOPROPYL ALCOHOL (UNII: ND2M416302)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0924-0243-00	1.35 mL in 1 PACKET; Type 0: Not a Combination Product	03/02/2022
2	NDC: 0924-0243-01	100 in 1 BOX	03/02/2022
2		1.35 mL 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 Drug	M003	03/02/2022

Labeler - Acme United Corporation (001180207)

Establishment
Name	Address	ID/FEI	Business Operations
Acme United Corporation		117825595	manufacture(0924-0243)