Aethusa Cynapium

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: Aethusa Cynapium
Generic name: AETHUSA CYNAPIUM
Manufacturer: OHM PHARMA INC.
Product type: HUMAN OTC DRUG
SPL set ID: a87ece85-5269-4dd4-8ece-a25392641702
SPL ID: d450946e-4255-8164-e053-2995a90a76c1
Version: 3
Effective date: 2021-12-29
Source export date: 2026-10-12
Source partition: 5
Source file: https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:41:08

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		Aethusa Cynapium	openfda.brand_name
generic name		AETHUSA CYNAPIUM	openfda.generic_name
manufacturer name		OHM PHARMA INC.	openfda.manufacturer_name
ndc	package	66096-780-01	openfda.package_ndc
ndc	product	66096-780	openfda.product_ndc
ndc11	package	66096078001	derived:openfda.package_ndc
spl id		d450946e-4255-8164-e053-2995a90a76c1	id
spl set id		a87ece85-5269-4dd4-8ece-a25392641702	set_id
unii		M6936L953C	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.