Home FDA labels 1b460000-2087-2f93-e063-6394a90adfe8 Allergena Dust Plus Mite 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 Allergena Dust Plus Mite
Generic name ECHINACEA, BAPTISIA TINCTORIA, HYDRASTIS CANADENSIS, MYRRHA, NASTURTIUM AQUATICUM, PHYTOLACCA DECANDRA, TRIGONELLA FOENUM-GRAECUM, BLATTA GERMANICA (GERMAN COCKROACH), DUST MITE (D.PTERONYSSINUS, D. FARINAE), PERIPLANETA AMERICANA, STANNUM METALLICUM
Manufacturer Meditrend, Inc. DBA Progena Professional Formulations
Product type HUMAN OTC DRUG
SPL set ID 95d66723-425e-44af-ab90-fa4d8368b7f7
SPL ID 1b460000-2087-2f93-e063-6394a90adfe8
Version 3
Effective date 2024-06-19
Source export date 2026-09-28
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/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:37:18 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 · 20 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Allergena Dust Plus Mite openfda.brand_name generic name ECHINACEA, BAPTISIA TINCTORIA, HYDRASTIS CANADENSIS, MYRRHA, NASTURTIUM AQUATICUM, PHYTOLACCA DECANDRA, TRIGONELLA FOENUM-GRAECUM, BLATTA GERMANICA (GERMAN COCKROACH), DUST MITE (D.PTERONYSSINUS, D. FARINAE), PERIPLANETA AMERICANA, STANNUM METALLICUM openfda.generic_name manufacturer name Meditrend, Inc. DBA Progena Professional Formulations openfda.manufacturer_name ndc package 62713-999-02 openfda.package_ndc ndc product 62713-999 openfda.product_ndc ndc11 package 62713099902 derived:openfda.package_ndc spl id 1b460000-2087-2f93-e063-6394a90adfe8 id spl set id 95d66723-425e-44af-ab90-fa4d8368b7f7 set_id unii 387GMG9FH5 openfda.unii unii 11E6VI8VEG openfda.unii unii 57L1Z5378K openfda.unii unii G9O67I0A8Q openfda.unii unii 487RI96K8Z openfda.unii unii 4N9P6CC1DX openfda.unii unii 2RQ1L9N089 openfda.unii unii ZW3Z11D0JV openfda.unii unii YH89GMV676 openfda.unii unii 5EF0HWI5WU openfda.unii unii JC71GJ1F3L openfda.unii unii PR9U2YPF3Q 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: Use Only as directed. Stop use and ask a doctor if symptoms worsen or do not improve after 5 days. If pregnant or breast-feeding , consult a health care professional before use.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.