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: 2026-09-28
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/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:49:49

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 9 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Kali Iodatum 1X	openfda.brand_name
generic name		KALI IODATUM.	openfda.generic_name
manufacturer name		OHM PHARMA INC.	openfda.manufacturer_name
ndc	package	66096-166-02	openfda.package_ndc
ndc	product	66096-166	openfda.product_ndc
ndc11	package	66096016602	derived:openfda.package_ndc
spl id		d44b323b-080a-b3d4-e053-2995a90aafb7	id
spl set id		682a651b-699d-45c6-8161-4b802cda1d7d	set_id
unii		1C4QK22F9J	openfda.unii

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.

Reported adverse events (FAERS/openFDA)#

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