MOZI-Q

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: MOZI-Q
Generic name: LEDUM PALUSTRE TWIG, URTICA URENS, SIMABA CEDRON SEED, DELPHINIUM STAPHISAGRIA SEED, GRINDELIA HIRSUTULA FLOWERING TOP
Manufacturer: Xerion Dispensary Ltd.
Product type: HUMAN OTC DRUG
SPL set ID: 63e62403-b45c-46c1-9c41-639c673d8204
SPL ID: 461831fc-bebe-bc73-e063-6294a90a30f5
Version: 10
Effective date: 2025-12-16
Source export date: 2026-10-27
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/2eee27992d1f29d82f827fd5be42f1314ed39ce4c497af5d81435ac6656a0957/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:24:54

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 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		MOZI-Q	openfda.brand_name
generic name		LEDUM PALUSTRE TWIG, URTICA URENS, SIMABA CEDRON SEED, DELPHINIUM STAPHISAGRIA SEED, GRINDELIA HIRSUTULA FLOWERING TOP	openfda.generic_name
manufacturer name		Xerion Dispensary Ltd.	openfda.manufacturer_name
ndc	package	53590-100-36	openfda.package_ndc
ndc	package	53590-100-60	openfda.package_ndc
ndc	product	53590-100	openfda.product_ndc
ndc11	package	53590010060	derived:openfda.package_ndc
ndc11	package	53590010036	derived:openfda.package_ndc
spl id		461831fc-bebe-bc73-e063-6294a90a30f5	id
spl set id		63e62403-b45c-46c1-9c41-639c673d8204	set_id
unii		877L01IZ0P	openfda.unii
unii		00543AP1JV	openfda.unii
unii		KHI40967MV	openfda.unii
unii		IHN2NQ5OF9	openfda.unii
unii		IDB0NAZ6AI	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 Stop use and ask a doctor if symptoms persist or worsen 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 immediately.

Reported adverse events (FAERS/openFDA)#

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