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.

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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 not finalpart333E07/09/2021
Labeler - Acme United Corporation (001180207)
Establishment
NameAddressID/FEIBusiness Operations
Acme United Corporation045924339relabel(0924-0245) , repack(0924-0245)
Establishment
NameAddressID/FEIBusiness Operations
Acme United Corporation080119599relabel(0924-0245) , repack(0924-0245)
Establishment
NameAddressID/FEIBusiness Operations
Acme United Corporation117825595manufacture(0924-0245)

Revised: 7/2021
Document Id: c6b4850d-cbf1-048d-e053-2995a90ab22d
Set id: c6b4850d-cbf0-048d-e053-2995a90ab22d
Version: 1
Effective Time: 20210709
 
Acme United Corporation