Home FDA labels f0513d8c-a844-4489-9173-35aee85736d9 Mold Antigens 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 Mold Antigens
Generic name ARSENICUM ALBUM, HISTAMINUM HYDROCHLORICUM, NATRUM SULPHURICUM, PHOSPHORUS, PULSATILLA (PRATENSIS), SEPIA, THUJA OCCIDENTALIS, ALTERNARIA TENUIS NEES, ASPERGILLUS NIGER, CANDIDA ALBICANS, CANDIDA PARAPSILOSIS, TORULA CEREVISIAE, MUCOR RACEMOSUS, RHIZOPUS NIGRICANS
Manufacturer Energique, Inc.
Product type HUMAN OTC DRUG
SPL set ID 881d9481-7c1f-45fc-a794-b7c43639daed
SPL ID f0513d8c-a844-4489-9173-35aee85736d9
Version 2
Effective date 2026-07-31
Source export date 2026-10-12
Source partition 11
Source file https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:45:10 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 · 22 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Mold Antigens openfda.brand_name generic name ARSENICUM ALBUM, HISTAMINUM HYDROCHLORICUM, NATRUM SULPHURICUM, PHOSPHORUS, PULSATILLA (PRATENSIS), SEPIA, THUJA OCCIDENTALIS, ALTERNARIA TENUIS NEES, ASPERGILLUS NIGER, CANDIDA ALBICANS, CANDIDA PARAPSILOSIS, TORULA CEREVISIAE, MUCOR RACEMOSUS, RHIZOPUS NIGRICANS openfda.generic_name manufacturer name Energique, Inc. openfda.manufacturer_name ndc package 44911-0702-1 openfda.package_ndc ndc product 44911-0702 openfda.product_ndc ndc11 package 44911070201 derived:openfda.package_ndc spl id f0513d8c-a844-4489-9173-35aee85736d9 id spl set id 881d9481-7c1f-45fc-a794-b7c43639daed set_id unii 27YLU75U4W openfda.unii unii 3POA0Q644U openfda.unii unii 0YPR65R21J openfda.unii unii QDL83WN8C2 openfda.unii unii 1NT28V9397 openfda.unii unii 4D7G21HDBC openfda.unii unii S7V92P67HO openfda.unii unii 17RH99LQ7G openfda.unii unii 978D8U419H openfda.unii unii 8E272251DI openfda.unii unii FEE198DK4Q openfda.unii unii 0KZ676D44N openfda.unii unii 52B29REC7H openfda.unii unii 9IOA40ANG6 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: Stop use and ask a doctor if symptoms persist for more than 7 days. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. DO NOT USE IF TAMPER EVIDENT SEAL IS BROKEN OR MISSING
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.