Baryta Iodata

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: Baryta Iodata
Generic name: BARYTA IODATA
Manufacturer: OHM PHARMA INC.
Product type: HUMAN OTC DRUG
SPL set ID: 8818cd88-0442-417f-a00c-aa2c837630ff
SPL ID: d450d9d2-55fe-494b-e053-2995a90ae369
Version: 3
Effective date: 2021-12-29
Source export date: 2026-10-27
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/2026-10-27/be847f9aea8d80a2cb7e9771acd1143be084664192ecf8f5be8ac1024116f4f0/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:17:36

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		Baryta Iodata	openfda.brand_name
generic name		BARYTA IODATA	openfda.generic_name
manufacturer name		OHM PHARMA INC.	openfda.manufacturer_name
ndc	package	66096-796-01	openfda.package_ndc
ndc	product	66096-796	openfda.product_ndc
ndc11	package	66096079601	derived:openfda.package_ndc
spl id		d450d9d2-55fe-494b-e053-2995a90ae369	id
spl set id		8818cd88-0442-417f-a00c-aa2c837630ff	set_id
unii		WKC4T7680A	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: Keep out of reach of children. If pregnant or breast-feeding, ask a health care professional before use. Stop use and ask a health care professional if symptoms persist for more than 3 days or worsen. Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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