Mertodol Solution

Manufacturer: Laboratorios Jaloma, S.A. de C.V.
Effective date: 2016-09-21
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-02 01:22:58

Label at a glance#

ProductMertodol Solution

Active ingredientBENZALKONIUM CHLORIDE

Label structure7 sections

Indications and uses

First aid to help prevent infection in *minor cuts *scrapes *burns

Dosage and administration

-Clean the affected area -Apply a small amount of this product on the area 1 to 3 times daily - May be covered with a sterile bandage

Label contents#

Full prescribing information#

Active Ingridients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

First aid to help prevent infection in *minor cuts *scrapes *burns

Warnings

WARNINGS SECTION

-For external use only

-Do not use in the eyes or apply over large areas of the body

Consult a doctor in case of

- deep or puncture wounds

-animal bites

-serious burns

-Stop use and consult a doctor if the condition persist or gets worse

-do not use longer than 1 week, unless directed by a doctor

Keep out of the reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediatley.

Directions.

DOSAGE & ADMINISTRATION SECTION

-Clean the affected area

-Apply a small amount of this product on the area 1 to 3 times daily

- May be covered with a sterile bandage

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Acetone, Alcohol, d & c red No. 22, water.

Labels

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

Mertodol Solution
Benzalkonium Chloride
ACETONE
WATER
D&C RED NO. 22
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
65055-202	65055-202-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ACETONE	1364PS73AF	IACT
WATER	059QF0KO0R	IACT
D&C RED NO. 22	1678RKX8RT	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
0022e63f-612f-29f0-e063-6294a90aff98			b0326803-dcad-4afc-9fa1-755ffbd6b58f	2023-07-10	Warnings	Exact identifier spl set id: b0326803-dcad-4afc-9fa1-755ffbd6b58f

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.