DDM Decolorized Iodine

Manufacturer
Discount Drug Mart | Pharma Nobis, LLC
Effective date
2023-12-19
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:04:56

Label at a glance#

ProductDDM Decolorized Iodine
Active ingredientALCOHOL
Label structure13 sections

Indications and uses

First aid to help prevent infection in minor cuts, scrapes and burns.

Dosage and administration

Clean the affected area. Aply a small amount to the affected area 1 to 3 times daily. May be covered with a sterile bandage. If bandaged, let it dry first.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Alcohol 45 % denatured with ammonia, Ammonium and Potassium Iodides.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

First aid to help prevent infection in minor cuts, scrapes and burns.

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.

Stop use and ask a doctor if:

OTC - STOP USE SECTION

The condition persists or gets worse, or if using this product for longer than 1 week.

When using this product:

OTC - WHEN USING SECTION

Do not use in the eyes. If contact occurs, flush with large amounts of water while lifting upper and lower lids. Do not apply over large areas of the body.

Keep out of the reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of acidental ingestion give milk, then give a starch solution made by mixing two tablespoonfools of cornstarch or flour to a pint of water. contact a poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Clean the affected area. Aply a small amount to the affected area 1 to 3 times daily. May be covered with a sterile bandage. If bandaged, let it dry first.

Inactive Ingredient:

INACTIVE INGREDIENT SECTION

Purified Water

Pther Information:

OTHER SAFETY INFORMATION

Will stain skin and clothing

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5f30b278-5791-4113-8781-878a9221ef8aProduct name220230125
2a70c781-a755-4d76-b20a-a958acfbdcdcProduct name220190619
304592ef-4a8a-4c22-8e8c-af73aa3d60e5Product name120180703
ac0821a1-ce75-4ea7-880a-59eecaecdf22Product name120180703
db5dc4f9-b907-46f6-8fb7-babcf04bbe5cProduct name120180619
41e9d6cf-3ed7-4c44-a57e-0685058d0896Product name120170824
5e652c92-68fd-426b-b0e7-5fc64e0b9f99Product name120170309
ddc0c11a-bba8-408f-b3c7-c4828b4bcc8cProduct name120150421

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53943-207-92DDM Decolorized Iodine59 mL in 1 BOTTLE, PLASTICLIQUID594

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53943-207DDM DECOLORIZED IODINE (ETHYL ALCOHOL) LIQUID [DISCOUNT DRUG MART]4Current NDC, Legacy NDC, 1 package rows20231220_5d570ea7-ab08-54b7-e053-2991aa0a7a83.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
53943-20753943-207-92

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
DDM Decolorized IodineETHYL ALCOHOLDiscount Drug Mart5d570ea7-ab08-54b7-e053-2991aa0a7a832023-12-19WarningsExact identifier
ndc (package): 53943-207-92
ndc (product): 53943-207
ndc11 (package): 53943020792
spl id: 0ce5eb71-362b-4afa-e063-6394a90af577
spl set id: 5d570ea7-ab08-54b7-e053-2991aa0a7a83

Reported adverse events (FAERS/openFDA)#

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