Home FDA labels 962a1d0f-8af9-4c0d-9cbd-0a9e5f4c981c Parasode 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 Parasode
Generic name ARTEMISIA VULGARIS ROOT, CHELIDONIUM MAJUS WHOLE, PUNICA GRANATUM ROOT BARK, SPIGELIA ANTHELMIA WHOLE, KRAMERIA LAPPACEA ROOT, ARSENIC TRIOXIDE, IRON, OYSTER SHELL CALCIUM CARBONATE, CRUDE, ARTEMISIA CINA PRE-FLOWERING TOP, SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS, GRAPHITE, CALOMEL, SODIUM CHLORIDE, AND SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
Manufacturer Zorex
Product type HUMAN OTC DRUG
SPL set ID 0ed722dc-cd25-4a15-b3f8-052cc7bcd9ec
SPL ID 962a1d0f-8af9-4c0d-9cbd-0a9e5f4c981c
Version 1
Effective date 2025-07-01
Source export date 2026-10-12
Source partition 7
Source file https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 01:59:47 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 Parasode openfda.brand_name generic name ARTEMISIA VULGARIS ROOT, CHELIDONIUM MAJUS WHOLE, PUNICA GRANATUM ROOT BARK, SPIGELIA ANTHELMIA WHOLE, KRAMERIA LAPPACEA ROOT, ARSENIC TRIOXIDE, IRON, OYSTER SHELL CALCIUM CARBONATE, CRUDE, ARTEMISIA CINA PRE-FLOWERING TOP, SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS, GRAPHITE, CALOMEL, SODIUM CHLORIDE, AND SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE openfda.generic_name manufacturer name Zorex openfda.manufacturer_name ndc package 81825-0012-1 openfda.package_ndc ndc product 81825-0012 openfda.product_ndc ndc11 package 81825001201 derived:openfda.package_ndc spl id 962a1d0f-8af9-4c0d-9cbd-0a9e5f4c981c id spl set id 0ed722dc-cd25-4a15-b3f8-052cc7bcd9ec set_id unii 28M1820ACT openfda.unii unii 7E889U5RNN openfda.unii unii J2D46N657D openfda.unii unii 4QQN74LH4O openfda.unii unii 451W47IQ8X openfda.unii unii 2E32821G6I openfda.unii unii S7V92P67HO openfda.unii unii WYT05213GE openfda.unii unii Y3V16D4PV4 openfda.unii unii P29ZH1A35Z openfda.unii unii CLV24I3T1D openfda.unii unii E1UOL152H7 openfda.unii unii 70WT22SF4B openfda.unii unii 32MP823R8S 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 Consult a physician for use in children under the age 12 years of age. IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use. KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact Poison Control Center right away. Do not use if TAMPER EVIDENT seal is broken or missing.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.