CVS MERTHIOLATE- benzalkonium chloride liquid 
CVS Pharmacy

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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CVS Merthiolate

CVS Merthiolate

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antiseptic

Indications

First aid antiseptic to help skin infection in minor: cuts, scrapes, burns, 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 the eyes

Apply over large areas of the body

Apply over raw surfaces or blistered areas

Use longer than one week unless directed by doctor.

Stop use and ask a doctor if

  • Redness, swelling or pain persists or increases.

Keep out of reach of children.

  • If swallowed, get medical help or contact a Poison Control Center immediately. Soap will deactivate the effects of this product.

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 dry first.
  • Children under 2 yrs. of age: Consult a doctor.

Inactive Ingredient

Acetone, FD&C Red No 4. Purified water.

PRINCIPAL DISPLAY PANEL

CVS
Merthiolate
Benzalkonium
Chloride 0.13%
Mercury free
2 FL OZ (59 mL)

PRINCIPAL DISPLAY PANEL CVS Merthiolate Benzalkonium Chloride 0.13% Mercury free 2 FL OZ (59 mL)

CVS MERTHIOLATE 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-749
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
ACETONE (UNII: 1364PS73AF)  
FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69842-749-9259 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2008
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/01/2008
Labeler - CVS Pharmacy (062312574)
Registrant - Humco Holding Group, inc. (825672884)
Establishment
NameAddressID/FEIBusiness Operations
Humco Holding Group, Inc.825672884analysis(69842-749) , manufacture(69842-749) , pack(69842-749) , label(69842-749)

Revised: 12/2020
Document Id: b6d998cb-998e-2226-e053-2a95a90aec39
Set id: dd498ab1-8350-41aa-86fc-2db57005f3e2
Version: 3
Effective Time: 20201219
 
CVS Pharmacy