Home NDC 81825-0012 Parasode
Product NDC 81825-0012
11-digit product format 818250012
Labeler code 81825
Product ID 81825-0012_962a1d0f-8af9-4c0d-9cbd-0a9e5f4c981c
Type HUMAN OTC DRUG
Nonproprietary 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
Dosage form LIQUID
Route ORAL
Labeler Zorex
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-06-27
Substance ARSENIC TRIOXIDE; ARTEMISIA CINA PRE-FLOWERING TOP; ARTEMISIA VULGARIS ROOT; CALOMEL; CHELIDONIUM MAJUS WHOLE; GRAPHITE; IRON; KRAMERIA LAPPACEA ROOT; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PUNICA GRANATUM ROOT BARK; SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SPIGELIA ANTHELMIA WHOLE
Active strength 6; 12; 4; 12; 4; 12; 9; 4; 12; 4; 12; 12; 12; 4 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Parasode
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ARTEMISIA VULGARIS ROOT 4 [hp_X]/mL CHELIDONIUM MAJUS WHOLE 4 [hp_X]/mL PUNICA GRANATUM ROOT BARK 4 [hp_X]/mL SPIGELIA ANTHELMIA WHOLE 4 [hp_X]/mL KRAMERIA LAPPACEA ROOT 4 [hp_X]/mL ARSENIC TRIOXIDE 6 [hp_X]/mL IRON 9 [hp_X]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/mL ARTEMISIA CINA PRE-FLOWERING TOP 12 [hp_X]/mL SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS 12 [hp_X]/mL GRAPHITE 12 [hp_X]/mL CALOMEL 12 [hp_X]/mL SODIUM CHLORIDE 12 [hp_X]/mL SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE 12 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 14 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 81825-0012-1 Parasode 30 mL in 1 BOTTLE, DROPPER LIQUID 30 1
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Parasode 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 Zorex 0ed722dc-cd25-4a15-b3f8-052cc7bcd9ec 2025-07-01 Warnings Exact identifier ndc (product): 81825-0012
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 81825-0012-1 81825001201 30 mL in 1 BOTTLE, DROPPER (81825-0012-1) 30 ml 2025-06-27 No No Current