MED NAP BENZALKONIUM CHLORIDE ANTISEPTIC- benzalkonium chloride liquid

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]

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 DOCTOR

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

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

QUESTIONS

1.800.835.2263

PRINCIPAL DISPLAY PANEL

Box Label

INGREDIENTS AND APPEARANCE

MED NAP BENZALKONIUM CHLORIDE ANTISEPTIC 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0924-0246
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0924-0246-00	1.35 mL in 1 PACKET; Type 0: Not a Combination Product	02/11/2022
2	NDC: 0924-0246-01	100 in 1 BOX	02/11/2022
2		1.35 mL in 1 PACKET; Type 0: Not a Combination Product
3	NDC: 0924-0246-02	1000 in 1 BOX	02/11/2022
3		1.35 mL in 1 PACKET; Type 0: Not a Combination Product
4	NDC: 0924-0246-03	12000 in 1 BOX	02/11/2022
4		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	02/11/2022

Labeler - Acme United Corporation (001180207)

Establishment
Name	Address	ID/FEI	Business Operations
Acme United Corporation		117825595	manufacture(0924-0246)