MERTHIOLATE- benzalkonium chloride liquid 
Humco Holding Group, Inc.

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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Private Label Merthiolate

Drug Facts

Active Ingredient

Benzalkonium chloride 0.13%

Purpose

Antiseptic

Uses

first aid to help prevent skin infection in minor cuts, scrapes, burns and insect bites.

Warnings

For external use only

Ask a doctor before use if you have

deep or puncture wounds, animal bites, serious burns.

When using this product

do not get into eyes. If contact occurs, rinse eyes throughly with water. do not apply over large areas of the body. do not use over raw surfaces or blistered areas. do not use longer than 1 week unless directed by a doctor.

Stop use and aska doctor if

condition persists or gets worse. symptoms clear up and occur again within a few days.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

adults and children 2 years and older. clean the affected area. apply a small amount on the area 1 to 3 times daily. may be covered with a sterile bandage. if bandaged, let it dry first. children under 2 years of age, do not use, consult a doctor.

Inactive ingredients

Alcohol 10%, Acetone, FD&C Red No 4, purified water

Quality Choice Label

QC

Premier Value

PV

DDM

DDM

CVS Label

CVC

Vida Mia Label

VM

MERTHIOLATE 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0395-9122
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
ACETONE (UNII: 1364PS73AF)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0395-9122-9259 mL in 1 BOTTLE; Type 0: Not a Combination Product11/14/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/25/1998
Labeler - Humco Holding Group, Inc. (825672884)
Registrant - Humco Holding Group, Inc. (825672884)
Establishment
NameAddressID/FEIBusiness Operations
Humco Holding Group, Inc.825672884manufacture(0395-9122) , analysis(0395-9122) , pack(0395-9122) , label(0395-9122)

Revised: 6/2020
Document Id: a885346e-a8e7-c83e-e053-2a95a90aa083
Set id: 60645c63-bb74-49ea-e053-2a91aa0aeea6
Version: 3
Effective Time: 20200620
 
Humco Holding Group, Inc.