PreQuimm

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
PreQuimm
Generic name
SILVER NITRATE,COLCHICUM AUTUMNALE BULB,CONIUM MACULATUM FLOWERING TOP,IPECAC,STRYCHNOS NUX VOMICA SEED,PULSATILLA PRATENSIS WHOLE,VERATRUM ALBUM ROOT
Manufacturer
ZRG Detox, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
6db848aa-bf72-466e-8bc8-d02d073ed120
SPL ID
42246a7e-5f14-68c0-e063-6394a90af8c6
Version
2
Effective date
2025-10-27
Source export date
2026-10-12
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:39:27
Harmonized routes table
Harmonized routes
SUBLINGUAL

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: If pregnant or nursing, ask a healthcare professional before use. Do not use if you have a known allergy to any ingredient in. If symptoms persist or worsen, consult your doctor. In case of overdose, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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