QUALITY CHOICE MERTHIOLATE- benzalkonium chloride liquid 
Chain Drug Market Association

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Quality Choice 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 ask a 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

Principal display panel

Label

image description

QUALITY CHOICE MERTHIOLATE 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-493
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:63868-493-0259 mL in 1 BOTTLE; Type 0: Not a Combination Product12/12/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00303/25/1998
Labeler - Chain Drug Market Association (011920774)
Registrant - Pharma Nobis, LLC (118564114)
Establishment
NameAddressID/FEIBusiness Operations
Pharma Nobis, LLC118564114analysis(63868-493) , manufacture(63868-493) , pack(63868-493) , label(63868-493)

Revised: 12/2023
Document Id: 0cf4bfe6-3853-e836-e063-6394a90ab8c3
Set id: 5b7303b9-b8c4-4e7c-876f-70ed76443055
Version: 5
Effective Time: 20231220
 
Chain Drug Market Association