Excitathyrotem

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
Excitathyrotem
Generic name
IODIUM, KALI IODATUM, HYPOTHALAMUS SUIS, HYPOPHYSIS SUIS, THYROIDINUM (SUIS), LITHIUM MURIATICUM, EPHEDRA VULGARIS
Manufacturer
Nucleic Products, LLC
Product type
HUMAN OTC DRUG
SPL set ID
c7c705a8-d7e6-4564-aa34-39da28e0b2dd
SPL ID
bd726e13-10c0-4d22-b023-fdc4815c0e52
Version
4
Effective date
2024-01-22
Source export date
2026-10-12
Source partition
14
Source file
https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/acb9b4700b9af1bdda1c389c7b35bfe38fd6d1a62aa48d17832812be4029b84f/drug-label-0014-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 03:12:43
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS: If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if seal is broken or missing. This Product does not contain sugar, starch, salt, preservatives, artificial flavors or additives, and no wheat, gluten, soy or milk derivatives.

Reported adverse events (FAERS/openFDA)#

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