Otc - Active Ingredient
iodine
Colloidal Iodine Solution
FDA Label NDC 69164-0003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Jci Colloidal Iodine Laboratory Co., Ltd. for the product Colloidal Iodine Solution (NDC 69164-0003). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
potassium iodide, hydrogen water
Otc - Purpose
increase level of immunity, digestive trouble
Otc - Keep Out Of Reach Of Children
keep out of reach of the children
Indications & Usage
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
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
for oral use only
Package Label.Principal Display Panel
Label (Label)
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