Home FDA labels d2ad486a-44c3-4ea5-b464-87dd6c02deff Systemic 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 Systemic Detox
Generic name BOLDO, CARDUUS MARIANUS, CHELIDONIUM MAJUS, SARSAPARILLA (SMILAX REGELII), GELSEMIUM SEMPERVIRENS, VERATRUM ALBUM, FERRUM METALLICUM, IODIUM, LYCOPODIUM CLAVATUM, NUX VOMICA, PULSATILLA (PRATENSIS), SELENIUM METALLICUM, THUJA OCCIDENTALIS, ZINCUM METALLICUM
Manufacturer Deseret Biologicals, Inc.
Product type HUMAN OTC DRUG
SPL set ID 8af4c01e-1d41-4e76-ba89-fa7908cd9098
SPL ID d2ad486a-44c3-4ea5-b464-87dd6c02deff
Version 2
Effective date 2022-10-11
Source export date 2026-10-27
Source partition 14
Source file https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-27/9122bd1bdced046e8f62ea012d80757473b7d83ea1faeea61faef490e06fd630/drug-label-0014-of-0014.json.zip
Source manifest SHA-256 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run 20261027T193451Z
Imported at 2026-10-27 21:09:58 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 · 22 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Systemic Detox openfda.brand_name generic name BOLDO, CARDUUS MARIANUS, CHELIDONIUM MAJUS, SARSAPARILLA (SMILAX REGELII), GELSEMIUM SEMPERVIRENS, VERATRUM ALBUM, FERRUM METALLICUM, IODIUM, LYCOPODIUM CLAVATUM, NUX VOMICA, PULSATILLA (PRATENSIS), SELENIUM METALLICUM, THUJA OCCIDENTALIS, ZINCUM METALLICUM openfda.generic_name manufacturer name Deseret Biologicals, Inc. openfda.manufacturer_name ndc package 43742-2052-1 openfda.package_ndc ndc product 43742-2052 openfda.product_ndc ndc11 package 43742205201 derived:openfda.package_ndc spl id d2ad486a-44c3-4ea5-b464-87dd6c02deff id spl set id 8af4c01e-1d41-4e76-ba89-fa7908cd9098 set_id unii 7E889U5RNN openfda.unii unii 269XH13919 openfda.unii unii 2H1576D5WG openfda.unii unii 1NT28V9397 openfda.unii unii 639KR60Q1Q openfda.unii unii U946SH95EE openfda.unii unii 9679TC07X4 openfda.unii unii Q4EWM09M3O openfda.unii unii 8E272251DI openfda.unii unii E1UOL152H7 openfda.unii unii J41CSQ7QDS openfda.unii unii QNS6W5US1Z openfda.unii unii C88X29Y479 openfda.unii unii H6241UJ22B 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. In case of overdose, contact a physician or Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use. Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.