Home FDA labels 8685fe17-ad92-4ce8-9894-2b457f1c1cb0 Cand Plus 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 Cand Plus
Generic name HYDRASTIS CANADENSIS, BERBERIS VULGARIS, BORAX, SACCHARUM OFFICINALE, CAFFEINUM, GALLICUM ACIDUM, INDOLUM, ALLIUM SATIVUM, ECHINACEA (ANGUSTIFOLIA), ASAFOETIDA, ACETALDEHYDE, FOLLICULINUM, LYCOPODIUM CLAVATUM, PHYTOLACCA DECANDRA, PULSATILLA (PRATENSIS), SEPIA, USTILAGO MAIDIS, TORULA CEREVISIAE
Manufacturer Deseret Biologicals, Inc.
Product type HUMAN OTC DRUG
SPL set ID 1f8ab864-27c2-4457-8ad7-5d65f9983e2c
SPL ID 8685fe17-ad92-4ce8-9894-2b457f1c1cb0
Version 6
Effective date 2024-03-06
Source export date 2026-10-12
Source partition 6
Source file https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 01:46:30 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 Cand Plus openfda.brand_name generic name HYDRASTIS CANADENSIS, BERBERIS VULGARIS, BORAX, SACCHARUM OFFICINALE, CAFFEINUM, GALLICUM ACIDUM, INDOLUM, ALLIUM SATIVUM, ECHINACEA (ANGUSTIFOLIA), ASAFOETIDA, ACETALDEHYDE, FOLLICULINUM, LYCOPODIUM CLAVATUM, PHYTOLACCA DECANDRA, PULSATILLA (PRATENSIS), SEPIA, USTILAGO MAIDIS, TORULA CEREVISIAE openfda.generic_name manufacturer name Deseret Biologicals, Inc. openfda.manufacturer_name ndc package 43742-1759-1 openfda.package_ndc ndc product 43742-1759 openfda.product_ndc ndc11 package 43742175901 derived:openfda.package_ndc spl id 8685fe17-ad92-4ce8-9894-2b457f1c1cb0 id spl set id 1f8ab864-27c2-4457-8ad7-5d65f9983e2c set_id unii GO1N1ZPR3B openfda.unii unii V1V998DC17 openfda.unii unii 3G6A5W338E openfda.unii unii 11E6VI8VEG openfda.unii unii C151H8M554 openfda.unii unii 4K7Z7K7SWG openfda.unii unii 8724FJW4M5 openfda.unii unii 91MBZ8H3QO openfda.unii unii 1TH8Q20J0U openfda.unii unii 48339473OT openfda.unii unii QDL83WN8C2 openfda.unii unii W9FZA51AS1 openfda.unii unii VB06AV5US8 openfda.unii unii 978D8U419H openfda.unii unii 2DI9HA706A openfda.unii unii 8E272251DI openfda.unii unii ZW3Z11D0JV openfda.unii unii C88X29Y479 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.