Home FDA labels 206776a9-35d9-4e97-9f68-37245b221d5e Spectric 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 Spectric
Generic name AGARICUS MUSCARIUS, ASPARTAME, BUFO RANA, CARCINOSIN, CEREBRUM SUIS, ETHYLICUM, HELLEBORUS NIGER, HYDROGEN, HYOSCYAMUS NIGER, KALI BROMATUM, L-DOPA, NEON, OLIBANUM (BOSWELLIA SERRATA), PLACENTA TOTALIS SUIS, SEROTONIN (HYDROCHLORIDE), STRAMONIUM, THUJA OCCIDENTALIS
Manufacturer Deseret Biologicals, Inc
Product type HUMAN OTC DRUG
SPL set ID 4ee7f979-c30d-4062-a453-27b6b0b38247
SPL ID 206776a9-35d9-4e97-9f68-37245b221d5e
Version 1
Effective date 2024-09-23
Source export date 2026-09-28
Source partition 10
Source file https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:07:21 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 · 25 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Spectric openfda.brand_name generic name AGARICUS MUSCARIUS, ASPARTAME, BUFO RANA, CARCINOSIN, CEREBRUM SUIS, ETHYLICUM, HELLEBORUS NIGER, HYDROGEN, HYOSCYAMUS NIGER, KALI BROMATUM, L-DOPA, NEON, OLIBANUM (BOSWELLIA SERRATA), PLACENTA TOTALIS SUIS, SEROTONIN (HYDROCHLORIDE), STRAMONIUM, THUJA OCCIDENTALIS openfda.generic_name manufacturer name Deseret Biologicals, Inc openfda.manufacturer_name ndc package 43742-2191-1 openfda.package_ndc ndc product 43742-2191 openfda.product_ndc ndc11 package 43742219101 derived:openfda.package_ndc spl id 206776a9-35d9-4e97-9f68-37245b221d5e id spl set id 4ee7f979-c30d-4062-a453-27b6b0b38247 set_id unii 4GB5DQR532 openfda.unii unii GKN429M9VS openfda.unii unii 7YNJ3PO35Z openfda.unii unii OSD78555ZM openfda.unii unii C8CV8867O8 openfda.unii unii 608DGJ6815 openfda.unii unii 1NT28V9397 openfda.unii unii DIF093I037 openfda.unii unii 4PW41QCO2M openfda.unii unii 4WRK2153H3 openfda.unii unii 4VB4Y46AHD openfda.unii unii Q59QU6N72Q openfda.unii unii C62OO7VD9K openfda.unii unii G6W4F0V8Z3 openfda.unii unii Z0H242BBR1 openfda.unii unii 46627O600J openfda.unii unii 3K9958V90M 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: If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away. Tamper Evident: 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.