FDA.reportPublic FDA data

Kali Iodatum 1X

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Kali Iodatum 1X
Generic name
KALI IODATUM.
Manufacturer
OHM PHARMA INC.
Product type
HUMAN OTC DRUG
SPL set ID
682a651b-699d-45c6-8161-4b802cda1d7d
SPL ID
d44b323b-080a-b3d4-e053-2995a90aafb7
Version
4
Effective date
2021-12-29
Source export date
2026-08-01
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/29baabee7fa6726d72190670d84f1571113181a958a8119cbe97e8f0d1d955b2/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:16:06
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS: THIS PRODUCT CONTAINS IODIDE. DO NOT TAKE IF YOU ARE HIPERSENSITIVE OR ALLERGIC TO IODIDE. IF YOU ARE PREGNANT OR BREAST-FEEDING,ask a health care professional before use. If symptoms worsen or persist for more than a week, discontinue use and contact a doctor. ​Keep out of reach of children.