FDA.reportPublic FDA data

JCI MN Colloidal Iodine Immune-improving Water

Manufacturer
JCI INSTITUTE OF MEDICAL SCIENCE
Effective date
2018-05-11
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 22:55:30

Label at a glance#

ProductJCI MN Colloidal Iodine Immune-improving Water
Active ingredientIODINE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

sodium iodide


INACTIVE INGREDIENT SECTION

potassium iodide, hydrogen water


OTC - PURPOSE SECTION

disinfection effect


OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children


INDICATIONS & USAGE SECTION

it is better to dose on an empty stomach
the dosage on undiluted solution is possibly recommended
do eat nothing within five minutes after the dosage
unit dose is 30ml
do take unit dose three times a day before each meal (morning, daylight, evening)
keep this dose guide for a month
if effective, do change the unit dose twice a day before each meal (morning, evening)
do discuss with your doctor for further dose


WARNINGS SECTION

do possibly avoid the food containing an antioxidant and color additives
do take the greatest possible care to eggs, milk, cheese and tuna
do take before meal. in case of other medicine dose, do take colloidal iodine within on hour before you take other medicine
do eat nothing within five minutes after the dosage
keep out of the direct sunlight


DOSAGE & ADMINISTRATION SECTION

oral use only


PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package insert
package insert

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
311093iodine 2 % Topical SolutionPSN4
311093iodine 20 MG/ML Topical SolutionSCD4
311093iodine 2 % tincture for Topical SolutionSY4
311093iodine 2 % Topical SolutionSY4

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
69164-4002-12020-01-31C16284748780-19d75b9d0-7d23-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69164-4002-1JCI MN Colloidal Iodine Immune-improving Water1000 mL in 1 BOTTLE, PLASTICSOLUTION10004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69164-4002JCI MN COLLOIDAL IODINE IMMUNE-IMPROVING WATER (IODINE) SOLUTION [JCI INSTITUTE OF MEDICAL SCIENCE]4Legacy NDC, 1 package rows20180512_2fd7057b-4e73-4fe2-9dbb-23a8015ad993.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
IODINEACTIVE INGREDIENT9679TC07X43
IODINEACTIVE MOIETY9679TC07X43
POTASSIUM IODIDEINACTIVE INGREDIENT1C4QK22F9J3
WATERINACTIVE INGREDIENT059QF0KO0R3

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69164-400269164-4002-1

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
POTASSIUM IODIDE1C4QK22F9JIACT
WATER059QF0KO0RIACT
IODINE9679TC07X4ACTIB

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
6bf86334-302c-707b-e053-2a91aa0aa5672fd7057b-4e73-4fe2-9dbb-23a8015ad9932018-05-11WarningsExact identifier
spl id: 6bf86334-302c-707b-e053-2a91aa0aa567
spl set id: 2fd7057b-4e73-4fe2-9dbb-23a8015ad993

Reported adverse events (FAERS/openFDA)#

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