DDM Merthiolate

Manufacturer
Discount Drug Mart | Humco Holding Group, Inc.
Effective date
2017-11-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:52:54

Label at a glance#

ProductDDM Merthiolate
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

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.

Label contents#

Full prescribing information#

DDM Merthiolate

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Indications

INDICATIONS & USAGE SECTION

First aid antiseptic to help skin infection in minor: cuts, scrapes, burns, insect bites.

Warnings

WARNINGS SECTION

For external use only.

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

Deep or puncture wounds

Animal bites

Serious burns

When using this product do not

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Redness, swelling or pain persists or increases.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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

INACTIVE INGREDIENT SECTION

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

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1049254benzalkonium chloride 0.13 % Topical SolutionPSN1
1049254benzalkonium chloride 1.3 MG/ML Topical SolutionSCD1
1049254benzalkonium chloride 0.13 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
53943-749-922022-07-29C16284748780-1e4f33bdf-9e63-d8a0-e053-dadaa90a6e4eDDM Merthiolate

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53943-749-92DDM Merthiolate59 mL in 1 BOTTLE, PLASTICLIQUID591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53943-749DDM MERTHIOLATE (BENZALKONIUM CHLORIDE) LIQUID [DISCOUNT DRUG MART]1Legacy NDC, 1 package rows20171107_5d56f88a-d8c4-3926-e053-2a91aa0a3ce9.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
53943-74953943-749-92

Ingredients#

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

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

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
5d56f88a-d8b7-3926-e053-2a91aa0a3ce95d56f88a-d8c4-3926-e053-2a91aa0a3ce92017-11-06WarningsExact identifier
spl id: 5d56f88a-d8b7-3926-e053-2a91aa0a3ce9
spl set id: 5d56f88a-d8c4-3926-e053-2a91aa0a3ce9

Reported adverse events (FAERS/openFDA)#

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