Home FDA labels 09e6e479-067c-43ec-8ab6-0df01a680ceb Cerebellutem 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 Cerebellutem
Generic name CAUSTICUM, ABSINTHIUM, RANUNCULUS GLACIALIS, THERIDION, HELODERMA, PICROTOXINUM, SUCCINUM, HELLEBORUS NIGER
Manufacturer Nucleic Products, LLC
Product type HUMAN OTC DRUG
SPL set ID 8212dd94-c963-4bcd-9fd6-fa25f51ebe55
SPL ID 09e6e479-067c-43ec-8ab6-0df01a680ceb
Version 4
Effective date 2025-04-08
Source export date 2026-09-28
Source partition 12
Source file https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:27:55 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 · 16 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Cerebellutem openfda.brand_name generic name CAUSTICUM, ABSINTHIUM, RANUNCULUS GLACIALIS, THERIDION, HELODERMA, PICROTOXINUM, SUCCINUM, HELLEBORUS NIGER openfda.generic_name manufacturer name Nucleic Products, LLC openfda.manufacturer_name ndc package 75053-0005-1 openfda.package_ndc ndc product 75053-0005 openfda.product_ndc ndc11 package 75053000501 derived:openfda.package_ndc spl id 09e6e479-067c-43ec-8ab6-0df01a680ceb id spl set id 8212dd94-c963-4bcd-9fd6-fa25f51ebe55 set_id unii DD5FO1WKFU openfda.unii unii ZLT174DL7U openfda.unii unii 14BZI1Z096 openfda.unii unii F84709P2XV openfda.unii unii O9M1UQ4YIO openfda.unii unii 608DGJ6815 openfda.unii unii 70J9Z0J26P openfda.unii unii 9Z8D3HEM8L 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: As with any drug, ask a doctor before use if pregnant or nursing. Consult a physician if: Symptoms persist for more than 7 days or worsen Keep this and all medications out of the reach of children. In case of accidental overdose, contact a medical professional or a poison Control Center immediately. Do not use if seal is broken or missing. This Product does not contain sugar, starch, preservatives, artificial flavors or additives, and no wheat, gluten, soy, or milk derivatives.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.