FDA.reportPublic FDA data

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
2026-08-01
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/2026-08-01/206e0852f7011b53c21719ec5c68ac6752381d0fcd1d348f7428adad64429e89/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:19:28
Harmonized routes table
Harmonized routes
ORAL

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.