Home FDA labels 9c1468ac-41c4-4d5b-a5d4-f0c2ab2f8e02 Party Detox 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 Party Detox
Generic name AGARICUS MUSCARIUS, AVENA SATIVA, BRYONIA, CARBO ANIMALIS, CARDUUS MARIANUS, CHELIDONIUM MAJUS, CINCHONA OFFICINALIS, HEPAR SUIS, KALI IODATUM, LAPIS ALBUS, NUX VOMICA, TARAXACUM OFFICINALE, THUJA OCCIDENTALIS
Manufacturer Liddell Laboratories, Inc.
Product type HUMAN OTC DRUG
SPL set ID 661646bf-acc1-4696-8a8e-2c9da38b4baa
SPL ID 9c1468ac-41c4-4d5b-a5d4-f0c2ab2f8e02
Version 3
Effective date 2024-11-04
Source export date 2026-10-12
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/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:14:42 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 · 23 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Party Detox openfda.brand_name generic name AGARICUS MUSCARIUS, AVENA SATIVA, BRYONIA, CARBO ANIMALIS, CARDUUS MARIANUS, CHELIDONIUM MAJUS, CINCHONA OFFICINALIS, HEPAR SUIS, KALI IODATUM, LAPIS ALBUS, NUX VOMICA, TARAXACUM OFFICINALE, THUJA OCCIDENTALIS openfda.generic_name manufacturer name Liddell Laboratories, Inc. openfda.manufacturer_name ndc package 50845-0252-2 openfda.package_ndc ndc package 50845-0252-1 openfda.package_ndc ndc product 50845-0252 openfda.product_ndc ndc11 package 50845025202 derived:openfda.package_ndc ndc11 package 50845025201 derived:openfda.package_ndc spl id 9c1468ac-41c4-4d5b-a5d4-f0c2ab2f8e02 id spl set id 661646bf-acc1-4696-8a8e-2c9da38b4baa set_id unii 7E889U5RNN openfda.unii unii 269XH13919 openfda.unii unii 39981FM375 openfda.unii unii 1NT28V9397 openfda.unii unii DIF093I037 openfda.unii unii U946SH95EE openfda.unii unii 2NVP93XVQ3 openfda.unii unii S003A158SB openfda.unii unii T7J046YI2B openfda.unii unii 1C4QK22F9J openfda.unii unii MA9CQJ3F7F openfda.unii unii 279O8I0433 openfda.unii unii 6EC706HI7F 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: Do not use if you have ever had an allergic reaction to this product or any of its ingredients. Stop use and ask a doctor if symptoms persist for more than 7 days, worsen, or if new symptoms occur. Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away. If pregnant or breast feeding, ask a health professional before use. Store at room temperature. Do not use is TAMPER EVIDENT seal around neck of bottle is missing or broken.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.