Home FDA labels 33e4e732-194d-4d0b-ba08-0ae14c3910f6 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 ETHYLICUM, KALI BROMATUM, ASPARTAME, L-DOPA, SEROTONIN (HYDROCHLORIDE), CEREBRUM SUIS, PLACENTA TOTALIS SUIS, AGARICUS MUSCARIUS, BUFO RANA, HELLEBORUS NIGER, HYOSCYAMUS NIGER, OLIBANUM (BOSWELLIA SERRATA), STRAMONIUM, THUJA OCCIDENTALIS, HELIUM, NEON, CARCINOSIN, HYDROGEN
Manufacturer Deseret Biologicals, Inc
Product type HUMAN OTC DRUG
SPL set ID d1981aca-de84-404d-8d38-3a013a531426
SPL ID 33e4e732-194d-4d0b-ba08-0ae14c3910f6
Version 3
Effective date 2024-09-11
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 01:59:40 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 · 26 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Spectric openfda.brand_name generic name ETHYLICUM, KALI BROMATUM, ASPARTAME, L-DOPA, SEROTONIN (HYDROCHLORIDE), CEREBRUM SUIS, PLACENTA TOTALIS SUIS, AGARICUS MUSCARIUS, BUFO RANA, HELLEBORUS NIGER, HYOSCYAMUS NIGER, OLIBANUM (BOSWELLIA SERRATA), STRAMONIUM, THUJA OCCIDENTALIS, HELIUM, NEON, CARCINOSIN, HYDROGEN openfda.generic_name manufacturer name Deseret Biologicals, Inc openfda.manufacturer_name ndc package 43742-2066-1 openfda.package_ndc ndc product 43742-2066 openfda.product_ndc ndc11 package 43742206601 derived:openfda.package_ndc spl id 33e4e732-194d-4d0b-ba08-0ae14c3910f6 id spl set id d1981aca-de84-404d-8d38-3a013a531426 set_id unii 4GB5DQR532 openfda.unii unii GKN429M9VS openfda.unii unii 7YNJ3PO35Z openfda.unii unii OSD78555ZM openfda.unii unii C8CV8867O8 openfda.unii unii 206GF3GB41 openfda.unii unii 608DGJ6815 openfda.unii unii 1NT28V9397 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 unii RQ7YY49K9Q 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.