FDA.reportPublic FDA data

LUGOLS SOLUTION

Manufacturer
Gordon Laboratories
Effective date
2010-02-01
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 20:12:25

Label at a glance#

ProductLUGOLS SOLUTION
Active ingredientIODINE
Label structure5 sections

Label contents#

Full prescribing information#

DESCRIPTION SECTION

Strong Iodine Solution USP a topical anti-infective agent.

HOW SUPPLIED SECTION


Applied with a q-tip.

SPL UNCLASSIFIED SECTION

May be stored at room temperature.

WARNINGS AND PRECAUTIONS SECTION

Single use only. Do not reuse.  Discard after one  use. Do not use if  seal is broken. Restricted to use by or on the order of a licensed Physician. Keep cap tightly sealed and product from light.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of Lugols LabelsImage of Lugols Labels

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
205228iodine 5 % / potassium iodide 10 % Topical SolutionPSN2
205228iodine 50 MG/ML / potassium iodide 100 MG/ML Topical SolutionSCD2
205228iodine 5 % / potassium iodide 10 % Topical SolutionSY2
205228Iodine 50 MG/ML / K+ Iodide 100 MG/ML Topical SolutionSY2
205228Iodine 50 MG/ML / Pot Iodide 100 MG/ML Topical SolutionSY2
205228Lugol's strong iodine 5 % / 10 % Topical SolutionSY2

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10481-0111-82019-10-29C16284748780-1960f7f55-bf33-8e05-e053-dbdaa90a074aLUGOLS SOLUTION

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10481-0111-8LUGOLS SOLUTION8 g in 1 BOTTLE, GLASSLIQUID82

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10481-0111LUGOLS SOLUTION (LUGOLS) LIQUID [GORDON LABORATORIES]2Legacy NDC, 1 package rows20110726_10b76538-eeeb-4886-b36c-922971fdf320.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
10481-0111-8ML - Milliliter10481-0111ba3b395a-c8aa-4304-a160-6941a483433712013-03-03

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
IODINEACTIVE INGREDIENT9679TC07X42
IODINEACTIVE MOIETY9679TC07X42
POTASSIUM IODIDEINACTIVE INGREDIENT1C4QK22F9J2
WATERINACTIVE INGREDIENT059QF0KO0R2

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10481-011110481-0111-8

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
IODINE9679TC07X4ACTIB
POTASSIUM IODIDE1C4QK22F9JIACT
WATER059QF0KO0RIACT

Source Document#

Source XML · Source PDF

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
48e2e8d2-dbcc-46b8-8e30-15931d5240d710b76538-eeeb-4886-b36c-922971fdf3202010-02-01WarningsExact identifier
spl id: 48e2e8d2-dbcc-46b8-8e30-15931d5240d7
spl set id: 10b76538-eeeb-4886-b36c-922971fdf320

Reported adverse events (FAERS/openFDA)#

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